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Configure Tracks on UCSC Genome Browser: Human Dec. 2013 (GRCh38/hg38)
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-   Mapping and Sequencing    
Base Position Chromosome position in bases. (Clicks here zoom in 3x)
p14 Fix Patches Reference Assembly Fix Patch Sequence Alignments
p14 Alt Haplotypes Reference Assembly Alternate Haplotype Sequence Alignments
Assembly Assembly from Fragments
Assembly #1 Assembly from Fragments (duplicate #1)
Centromeres Centromere Locations
Chromosome Band Chromosome Bands Localized by FISH Mapping Clones
Clone Ends Mapping of clone libraries end placements
Exome Probesets Exome Capture Probesets and Targeted Region
FISH Clones Clones Placed on Cytogenetic Map Using FISH
FISH Clones #1 Clones Placed on Cytogenetic Map Using FISH (duplicate #1)
Gap Gap Locations
GC Percent GC Percent in 5-Base Windows
GRC Contigs Genome Reference Consortium Contigs
GRC Contigs ctgPos2 (duplicate #1)
GRC Incident GRC Incident Database
Hg19 Diff Contigs New to GRCh38/(hg38), Not Carried Forward from GRCh37/(hg19)
INSDC Accession at INSDC - International Nucleotide Sequence Database Collaboration
INSDC ucscToINSDC (duplicate #1)
LiftOver & ReMap UCSC LiftOver and NCBI ReMap: Genome alignments to convert annotations to hg19
LRG Regions Locus Reference Genomic (LRG) / RefSeqGene Sequences Mapped to Dec. 2013 (GRCh38/hg38) Assembly
LRG Regions lrg (duplicate #1)
Mappability Hoffman Lab Umap and Bismap Mappability
     Umap     Single-read and multi-read mappability by Umap
     Bismap     Single-read and multi-read mappability after bisulfite conversion
Problematic Regions Problematic/special genomic regions for sequencing or very variable regions
     Problematic Regions     Problematic/special genomic regions for sequencing or very variable regions
     Highly Reproducible Regions     Highly Reproducible genomic regions for sequencing
Recomb Rate Recombination rate: Genetic maps from deCODE and 1000 Genomes
     Recomb. 1k Genomes     Recombination rate: 1000 Genomes, lifted from hg19 (PR Loh)
     Recomb. deCODE Dmn     Recombination rate: De-novo mutations found in deCODE samples
     Recomb. deCODE Evts     Recombination events in deCODE Genetic Map (zoom to < 10kbp to see the events)
     Recomb. deCODE Mat     Recombination rate: deCODE Genetics, maternal
     Recomb. deCODE Pat     Recombination rate: deCODE Genetics, paternal
     Recomb. deCODE Avg     Recombination rate: deCODE Genetics, average from paternal and maternal (mat for chrX)
RefSeq Acc RefSeq Accession
Restr Enzymes Restriction Enzymes from REBASE
Scaffolds GRCh38 Defined Scaffold Identifiers
Short Match Perfect Matches to Short Sequence ()
STS Markers STS Markers on Genetic (blue) and Radiation Hybrid (black) Maps
-   Genes and Gene Predictions    
GENCODE V44 GENCODE V44
GENCODE V44 knownGene (duplicate #1)
NCBI RefSeq RefSeq genes from NCBI
CCDS Consensus CDS
CRISPR Targets CRISPR/Cas9 -NGG Targets, whole genome
CRISPR Targets crisprAllTargets (duplicate #1)
updated GENCODE Versions Container of all new and previous GENCODE releases
     GENCODE V20 (Ensembl 76)     Gene Annotations from GENCODE Version 20 (Ensembl 76)
     All GENCODE V22     All GENCODE transcripts including comprehensive set V22
     All GENCODE V23     All GENCODE transcripts including comprehensive set V23
     All GENCODE V24     All GENCODE transcripts including comprehensive set V24
     All GENCODE V25     All GENCODE transcripts including comprehensive set V25
     All GENCODE V26     All GENCODE annotations from V26 (Ensembl 88)
     All GENCODE V27     All GENCODE annotations from V27 (Ensembl 90)
     All GENCODE V28     All GENCODE annotations from V28 (Ensembl 92)
     All GENCODE V29     All GENCODE annotations from V29 (Ensembl 94)
     All GENCODE V30     All GENCODE annotations from V30 (Ensembl 96)
     All GENCODE V31     All GENCODE annotations from V31 (Ensembl 97)
     All GENCODE V32     All GENCODE annotations from V32 (Ensembl 98)
     All GENCODE V33     All GENCODE annotations from V33 (Ensembl 99)
     All GENCODE V34     All GENCODE annotations from V34 (Ensembl 100)
     All GENCODE V35     All GENCODE annotations from V35 (Ensembl 101)
     All GENCODE V36     All GENCODE annotations from V36 (Ensembl 102)
     All GENCODE V37     All GENCODE annotations from V37 (Ensembl 103)
     All GENCODE V38     All GENCODE annotations from V38 (Ensembl 104)
     All GENCODE V39     All GENCODE annotations from V39 (Ensembl 105)
     All GENCODE V40     All GENCODE annotations from V40 (Ensembl 106)
     All GENCODE V41     All GENCODE annotations from V41 (Ensembl 107)
     All GENCODE V42     All GENCODE annotations from V42 (Ensembl 108)
     All GENCODE V43     All GENCODE annotations from V43 (Ensembl 109)
     All GENCODE V44     All GENCODE annotations from V44 (Ensembl 110)
    new All GENCODE V45     All GENCODE annotations from V45 (Ensembl 111)
HGNC HUGO Gene Nomenclature
IKMC Genes Mapped International Knockout Mouse Consortium Genes Mapped to Human Genome
LRG Transcripts Locus Reference Genomic (LRG) / RefSeqGene Fixed Transcript Annotations
MANE NCBI RefSeq & Ensembl transcripts from MANE: most relevant transcript for every protein-coding gene gene
MGC Genes Mammalian Gene Collection Full ORF mRNAs
MGC Genes mgcFullMrna (duplicate #1)
Non-coding RNA RNA sequences that do not code for a protein
     tRNA Genes     Transfer RNA Genes Identified with tRNAscan-SE
     sno/miRNA     C/D and H/ACA Box snoRNAs, scaRNAs, and microRNAs from snoRNABase and miRBase
     lincRNA TUCP     lincRNA and TUCP transcripts
     lincRNA RNA-Seq     lincRNA RNA-Seq reads expression abundances
Old UCSC Genes Previous Version of UCSC Genes
ORFeome Clones ORFeome Collaboration Gene Clones
Other RefSeq Non-Human RefSeq Genes
Other RefSeq #1 Non-Mouse RefSeq Genes (duplicate #1)
Other RefSeq #2 Non-Mouse RefSeq Genes (duplicate #2)
Pfam in GENCODE Pfam Domains in GENCODE Genes
Pfam in GENCODE ucscGenePfam (duplicate #1)
Pfam in GENCODE dup_0_ucscGenePfam (duplicate #2)
Prediction Archive Gene Prediction Archive
     SGP Genes     sgpGene (duplicate #1)
     Genscan Genes #1     Genscan Gene Predictions (duplicate #1)
     Geneid Genes     geneid (duplicate #1)
     SIB Genes     Swiss Institute of Bioinformatics Gene Predictions from mRNA and ESTs
     SGP Genes     SGP Gene Predictions Using Mouse/Human Homology
     Genscan Genes     Genscan Gene Predictions
     Geneid Genes     Geneid Gene Predictions
     AUGUSTUS     AUGUSTUS ab initio gene predictions v3.1
RetroGenes V9 Retroposed Genes V9, Including Pseudogenes
TransMap V5 TransMap Alignments Version 5
     TransMap ESTs     TransMap EST Mappings Version 5
     TransMap RNA     TransMap GenBank RNA Mappings Version 5
     TransMap RefGene     TransMap RefSeq Gene Mappings Version 5
     TransMap Ensembl     TransMap Ensembl and GENCODE Mappings Version 5
UCSC Alt Events Alternative Splicing, Alternative Promoter and Similar Events in UCSC Genes
UCSC Alt Events #1 Alternative Splicing, Alternative Promoter and Similar Events in UCSC Genes (duplicate #1)
UniProt UniProt SwissProt/TrEMBL Protein Annotations
-   Phenotype and Literature    
OMIM Alleles OMIM Allelic Variant Phenotypes
OMIM Alleles #1 OMIM Allelic Variant Phenotypes (duplicate #1)
COVID Rare Harmful Var Rare variants underlying COVID-19 severity and susceptibility from the COVID Human Genetics Effort
COVID Rare Harmful Var #1 Rare variants underlying COVID-19 severity and susceptibility from the COVID Human Genetics Effort (duplicate #1)
new AbSplice Scores Aberrant Splicing Prediction Scores
new AbSplice Scores abSplice (duplicate #1)
CADD CADD 1.6 Score for all single-basepair mutations and selected insertions/deletions
     Insertions     CADD 1.6 Score: Insertions - label is length of insertion
     Deletions     CADD 1.6 Score: Deletions - label is length of deletion
     CADD     CADD 1.6 Score for all possible single-basepair mutations (zoom in for scores)
Cancer Gene Expr Gene Expression in 33 TCGA Cancer Tissues (GENCODE v23)
     Cancer Transc Expr     Transcript-level Expression in 33 TCGA Cancer Tissues (GENCODE v23)
     Cancer Gene Expr     Gene Expression in 33 TCGA Cancer Tissues (GENCODE v23)
ClinGen ClinGen curation activities (Dosage Sensitivity and Gene-Disease Validity)
ClinGen CNVs Clinical Genome Resource (ClinGen) CNVs
ClinVar Variants ClinVar Variants
Constraint scores Human constraint scores
     UKB Depl. Rank Score     UK Biobank / deCODE Genetics Depletion Rank Score
     HMC     HMC - Homologous Missense Constraint Score on PFAM domains
     JARVIS     JARVIS: score to prioritize non-coding regions for disease relevance
Coriell CNVs Coriell Cell Line Copy Number Variants
COSMIC Catalogue of Somatic Mutations in Cancer V98
COSMIC Regions Catalogue of Somatic Mutations in Cancer V82
DECIPHER CNVs DECIPHER CNVs
DECIPHER CNVs decipher (duplicate #1)
DECIPHER SNVs DECIPHER: Chromosomal Imbalance and Phenotype in Humans (SNVs)
Development Delay Copy Number Variation Morbidity Map of Developmental Delay
new Dosage Sensitivity pHaplo and pTriplo dosage sensitivity map from Collins et al 2022
GenCC The Gene Curation Coalition Annotations
GenCC genCC (duplicate #1)
Gene Interactions Protein Interactions from Curated Databases and Text-Mining
GeneReviews GeneReviews
GWAS Catalog NHGRI-EBI Catalog of Published Genome-Wide Association Studies
HGMD public Human Gene Mutation Database - Public Version Dec 2022
LOVD Variants Leiden Open Variation Database Public Variants
OMIM Cyto Loci OMIM Cytogenetic Loci Phenotypes - Gene Unknown
OMIM Genes OMIM Gene Phenotypes - Dark Green Can Be Disease-causing
Orphanet Orphadata: Aggregated Data From Orphanet
Orphanet #1 Orphadata: Aggregated Data From Orphanet (duplicate #1)
PanelApp Genomics England PanelApp Diagnostics
REVEL Scores REVEL Pathogenicity Score for single-base coding mutations (zoom for exact score)
SNPedia SNPedia
TCGA Pan-Cancer TCGA Pan-Cancer mutations: 33 TCGA Cancer Projects Summary (Pan-Can 33)
UniProt Variants UniProt/SwissProt Amino Acid Substitutions
updated Variants in Papers Genetic Variants mentioned in scientific publications
     Mastermind Variants     Genomenon Mastermind Variants extracted from full text publications
    new Avada Variants     Avada Variants extracted from full text publications
-   Human Pangenome - HPRC    
new Multiple Alignment Multiple Alignment on 90 human genome assemblies
new Pairwise Alignments Human Genomes, Chain/Net pairwise alignments, as mapped by the HPRC project
new Rearrangements Rearrangements including indels, inversions, and duplications
new Short Variants Short Variants
     HPRC Variants > 3bp     HPRC VCF variants filtered for items size > 3bp
     HPRC Variants <= 3bp     HPRC VCF variants filtered for items size <= 3bp
     HPRC All Variants     HPRC variants decomposed from hprc-v1.0-mc.grch38.vcfbub.a100k.wave.vcf.gz (Liao et al 2023), no size filtering
-   Single Cell RNA-seq    
Blood (PBMC) Hao Peripheral blood mononuclear cells (PBMC) from Hao et al 2020
     Blood PBMC Time     Blood PBMCs binned by time into experiment from Hao et al 2020
     Blood PBMC Phase     Blood PBMCs binned by phase of cell cycle from Hao et al 2020
     Blood PBMC Donor     Blood PBMCs binned by blood donor from Hao et al 2020
     Blood PBMC Cells 3     Blood PBMCs binned by cell type (level 3) from Hao et al 2020
     Blood PBMC Cells 2     Blood PBMCs binned by cell type (level 2) from Hao et al 2020
     Blood PBMC Cells     Blood (PBMCs) binned by cell type (level 1) from Hao et al 2020
Colon Wang Colon single cell sequencing from Wang et al 2020
     Colon Donor     Colon cells binned by organ donor from Wang et al 2020
     Colon Cells     Colon cells binned by cell type from Wang et al 2020
Cortex Velmeshev Cerebral cortex single cell data from Velmeshev et al 2019
     Cortex Sex     Cerebral cortex RNA binned by sex of donor from Velmeshev et al 2019
     Cortex Sample     Cerebral cortex RNA binned by biosample from Velmeshev et al 2019
     Cortex Donor     Cerebral cortex RNA binned by organ donor from Velmeshev et al 2019
     Cortex Diagnosis     Cerebral cortex RNA binned by ASD/control diagnosis from Velmeshev et al 2019
     Cortex Cells     Cerebral cortex RNA binned by cell type from Velmeshev et al 2019
Cross Tissue Nuclei Single Nuclei sequenced across many tissues
     GTEx Immune Atlas     GTEx single nuclei immune expression
     Cross Tissue Details     Cross tissue nuclei full details
     Cross Tissue Nuclei     Cross tissue nuclei RNA by tissue and cell type
Fetal Gene Atlas Fetal Gene Atlas from Cao et al 2020
     Fetal Sex     Fetal Gene Atlas binned by sex from Cao et al 2020
     Fetal RT Group     Fetal Gene Atlas binned by RT group from Cao et al 2020
     Fetal Organ     Fetal Gene Atlas binned by organ from Cao et al 2020
     Fetal Lineage     Fetal Gene Atlas binned by cell lineage and organ from Cao et al 2020
     Fetal Exp     Fetal Gene Atlas binned by experiment id from Cao et al 2020
     Fetal Donor ID     Fetal Gene Atlas binned by donor ID from Cao et al 2020
     Fetal Cells     Fetal Gene Atlas binned by cell type from Cao et al 2020
     Fetal Assay     Fetal Gene Atlas binned by assay (cell/nucleus) from Cao et al 2020
Heart Cell Atlas Heart single cell RNA data from https://heartcellatlas.com
     Heart HCA Version     Heart cell RNA binned by 10x chemistry version from https://heartcellatlas.org
     Heart HCA State     Heart cell RNA binned by cell state from https://heartcellatlas.org
     Heart HCA Source     Heart cell RNA binned by source (nucleus vs whole cell) from https://heartcellatlas.org
     Heart HCA Sex     Heart cell RNA binned by sex of donor from https://heartcellatlas.org
     Heart HCA Sample     Heart cell RNA binned by biosample from https://heartcellatlas.org
     Heart HCA Region     Heart cell RNA binned by region of collection from https://heartcellatlas.org
     Heart HCA Donor     Heart cell RNA binned by organ donor from https://heartcellatlas.org
     Heart HCA Cells     Heart cell RNA binned by cell type from https://heartcellatlas.org
     Heart HCA Age     Heart cell RNA binned by age group of donor from https://heartcellatlas.org
Ileum Wang Ileum single cell sequencing from Wang et al 2020
     Ileum Donor     Ileum cells binned by organ donor from Wang et al 2020
     Ileum Cells     Ileum cells binned by cell type from Wang et al 2020
Kidney Stewart Kidney single cell data from Stewart et al 2019
     Kidney Project     Kidney RNA binned by project from Stewart et al 2019
     Kidney Experiment     Kidney RNA binned by Experiment from Stewart et al 2019
     Kidney Details     Kidney RNA binned by detailed cell type from Stewart et al 2019
     Kidney Compartment     Kidney RNA binned by compartment from Stewart et al 2019
     Kidney Cells     Kidney RNA binned by merged cell type from Stewart et al 2019
     Kidney Broad CT     Kidney RNA binned by broad cell type from Stewart et al 2019
Liver MacParland Liver single cell sequencing from MacParland et al 2018
     Liver Donor     Liver cells binned by organ donor from MacParland et al 2018
     Liver Cells     Liver cells binned by cell type from MacParland et al 2018
     Liver Broad     Liver cells binned by broad cell type from MacParland et al 2018
Lung Travaglini Lung cells from from Travaglini et al 2020
     Lung Sample FACS     Lung cells FACS method binned by sample from Travaglini et al 2020
     Lung Sample     Lung cells 10x method binned by sample from Travaglini et al 2020
     Lung Organ FACS     Lung cells FACS method binned by organ from Travaglini et al 2020
     Lung Organ     Lung cells 10x method binned by organ from Travaglini et al 2020
     Lung Mag Sel     Lung cells 10x method binned by magnetic.selection from Travaglini et al 2020
     Lung Locat FACS     Lung cells FACS method binned by location from Travaglini et al 2020
     Lung Locat     Lung cells 10x method binned by location from Travaglini et al 2020
     Lung Label FACS     Lung cells FACS method binned by label from Travaglini et al 2020
     Lung Half Det FACS     Lung cells FACS method binned by merged cell type from Travaglini et al 2020
     Lung Half Det     Lung cells 10x method binned by halfway detailed cell type from Travaglini et al 2020
     Lung Gating FACS     Lung cells FACS method binned by gating from Travaglini et al 2020
     Lung Donor FACS     Lung cells FACS method binned by organ donor from Travaglini et al 2020
     Lung Donor     Lung cells 10x method binned by organ donor from Travaglini et al 2020
     Lung Detail FACS     Lung cells FACS method binned by detailed cell type from Travaglini et al 2020
     Lung Detail     Lung cells 10x method binned by detailed cell type from Travaglini et al 2020
     Lung Compart FACS     Lung cells FACS method binned by compartment from Travaglini et al 2020
     Lung Compart     Lung cells 10x method binned by compartment from Travaglini et al 2020
     Lung Cells FACS     Lung cells FACS method binned by merged cell type from Travaglini et al 2020
     Lung Cells     Lung cells 10x method binned by merged cell type from Travaglini et al 2020
Merged Cells Single cell RNA expression levels cell types from many organs
Muscle De Micheli Muscle single cell data from De Micheli et al 2020
     Muscle Sample     Muscle RNA binned by biosample from De Micheli et al 2020
     Muscle Cells     Muscle RNA binned by cell type from De Micheli et al 2020
Pancreas Baron Pancreas single cell sequencing from Baron et al 2016
     Pancreas Donor     Pancreas cells binned by organ donor from Baron et al 2016
     Pancreas Details     Pancreas cells binned by detailed cell type from Baron et al 2016
     Pancreas Cells     Pancreas cells binned by cell type from Baron et al 2016
     Pancreas Batch     Pancreas cells binned by batch from Baron et al 2016
Placenta Vento-Tormo Placenta and decidua cells from from Vento-Tormo et al 2018
     Placenta Stage     Placenta and decidua cells binned by placental stage 10x from Vento-Tormo et al 2018
     Placenta Mat/Fet Ss2     Placenta and decidua cells binned by maternal/fetal smart-seq2 from Vento-Tormo et al 2018
     Placenta Mat/Fet     Placenta and decidua cells binned by maternal/fetal 10x from Vento-Tormo et al 2018
     Placenta Loc Ss2     Placenta and decidua cells binned by cell location smart-seq2 from Vento-Tormo et al 2018
     Placenta Loc     Placenta and decidua cells binned by cell location 10x from Vento-Tormo et al 2018
     Placenta Detail Ss2     Placenta and decidua cells binned by detailed cell type smart-seq2 from Vento-Tormo et al 2018
     Placenta Detail     Placenta and decidua cells binned by detailed cell type 10x from Vento-Tormo et al 2018
     Placenta Cells Ss2     Placenta and decidua cells binned by cell type smart-seq2 from Vento-Tormo et al 2018
     Placenta Cells     Placenta and decidua cells binned by cell type 10x from Vento-Tormo et al 2018
Rectum Wang Rectum single cell sequencing from Wang et al 2020
     Rectum Donor     Rectum cells binned by organ donor from Wang et al 2020
     Rectum Cells     Rectum cells binned by cell type from Wang et al 2020
Skin Sole-Boldo Skin single cell data from Sole-Boldo et al 2020
     Skin Donor     Skin single cell RNA binned by skin donor from Sole-Boldo et al 2020
     Skin Cell+Age     Skin single cell RNA binned by cell type and donor's age from Sole-Boldo et all 2020
     Skin Cell     Skin single cell RNA binned by cell type from Sole-Boldo et al 2020
     Skin Age     Skin single cell RNA binned by skin donor's age from Sole-Boldo et al 2020
Tabula Sapiens Tabula Sapiens single cell RNA data from many tissues
     Tabula Tissue Cell     Tabula sapiens RNA by tissue and cell type
     Tabula Details     Tabula sapiens full details view
-   mRNA and EST    
Human ESTs Human ESTs Including Unspliced
Human mRNAs Human mRNAs from GenBank
Human mRNAs #1 Human mRNAs from GenBank (duplicate #1)
Mouse mRNAs #2 Mouse mRNAs from GenBank (duplicate #2)
Other ESTs Non-Human ESTs from GenBank
Other mRNAs Non-Human mRNAs from GenBank
Other mRNAs xenoMrna (duplicate #2)
Other mRNAs #1 Non-Mouse mRNAs from GenBank (duplicate #1)
SIB Alt-Splicing Alternative Splicing Graph from Swiss Institute of Bioinformatics
Spliced ESTs Human ESTs That Have Been Spliced
-   Expression    
GTEx Gene V8 Gene Expression in 54 tissues from GTEx RNA-seq of 17382 samples, 948 donors (V8, Aug 2019)
GTEx RNA-Seq Coverage GTEx V8 RNA-Seq Read Coverage by Tissue
Affy Archive Affymetrix Archive
     Affy U95     Alignments of Affymetrix Consensus/Exemplars from HG-U95
     Affy U133     Alignments of Affymetrix Consensus/Exemplars from HG-U133
     Affy GNF1H     Alignments of Affymetrix Consensus/Exemplars from GNF1H
EPDnew Promoters Promoters from EPDnew
GNF Atlas 2 GNF Expression Atlas 2
GTEx Gene Gene Expression in 53 tissues from GTEx RNA-seq of 8555 samples (570 donors)
GTEx Transcript Transcript Expression in 53 tissues from GTEx RNA-seq of 8555 samples/570 donors
GTEx Transcript gtexTranscExpr (duplicate #2)
GTEx Transcript #1 Transcript Expression in 53 tissues from GTEx RNA-seq of 8555 samples/570 donors (duplicate #1)
GWIPS-viz Riboseq Ribosome Profiling from GWIPS-viz
miRNA Tissue Atlas Tissue-Specific microRNA Expression from Two Individuals
-   Regulation    
ENCODE cCREs ENCODE Candidate Cis-Regulatory Elements (cCREs) combined from all cell types
ENCODE cCREs encodeCcreCombined (duplicate #1)
ENCODE Regulation Integrated Regulation from ENCODE
     TF ChIP     Transcription Factor ChIP-seq Peaks (340 factors in 129 cell types) from ENCODE 3
     TF Clusters     Transcription Factor ChIP-seq Clusters (340 factors, 129 cell types) from ENCODE 3
     DNase HS     DNase I Hypersensitivity in 95 cell types from ENCODE
     DNase Signal     DNase I Hypersensitivity Signal Colored by Similarity from ENCODE
     DNase Clusters     DNase I Hypersensitivity Peak Clusters from ENCODE (95 cell types)
     Layered H3K27Ac     H3K27Ac Mark (Often Found Near Regulatory Elements) on 7 cell lines from ENCODE
     Layered H3K4Me3     H3K4Me3 Mark (Often Found Near Promoters) on 7 cell lines from ENCODE
     Layered H3K4Me1     H3K4Me1 Mark (Often Found Near Regulatory Elements) on 7 cell lines from ENCODE
     Transcription     Transcription Levels Assayed by RNA-seq on 9 Cell Lines from ENCODE
CpG Islands CpG Islands (Islands < 300 Bases are Light Green)
     Unmasked CpG     CpG Islands on All Sequence (Islands < 300 Bases are Light Green)
     CpG Islands     CpG Islands (Islands < 300 Bases are Light Green)
new FANTOM5 FANTOM5: Mapped transcription start sites (TSS) and their usage
     TSS activity (TPM)     FANTOM5: TSS activity per sample (TPM)
     TSS activity - read counts     FANTOM5: TSS activity per sample read counts
     Max counts of CAGE reads     FANTOM5: Max counts of CAGE reads
     Total counts of CAGE reads     FANTOM5: Total counts of CAGE reads
     TSS peaks     FANTOM5: DPI peak, robust set
GeneHancer GeneHancer Regulatory Elements and Gene Interactions
GTEx cis-eQTLs GTEx fine-mapped cis-eQTLs
Hi-C and Micro-C Comparison of Micro-C and In situ Hi-C protocols in H1-hESC and HFFc6
updated JASPAR Transcription Factors JASPAR Transcription Factor Binding Site Database
ORegAnno Regulatory elements from ORegAnno
ORegAnno #1 Regulatory elements from ORegAnno (duplicate #1)
RefSeq Func Elems NCBI RefSeq Functional Elements
ReMap ChIP-seq ReMap Atlas of Regulatory Regions
VISTA Enhancers VISTA Enhancers
VISTA Enhancers vistaEnhancersBb (duplicate #1)
-   Comparative Genomics    
Conservation Vertebrate Multiz Alignment & Conservation (100 Species)
Cactus 241-way Cactus Alignment & Conservation of Zoonomia Placental Mammals (241 Species)
Cons 30 Primates Mammals Multiz Alignment & Conservation (27 primates)
Primate Chain/Net Primate Genomes, Chain and Net Alignments
Placental Chain/Net Non-primate Placental Mammal Genomes, Chain and Net Alignments
Vertebrate Chain/Net Non-placental Vertebrate Genomes, Chain and Net Alignments
Cactus 447-way Cactus Alignment & Conservation on 447 mammal species, including Zoonomia genomes
CHM13 alignments CHM13 (GCA_009914755.4) v1_nfLO liftOver alignments
Multiz 470-way Multiz Alignment & Conservation (470 mammals)
-   Variation    
dbSNP 155 Short Genetic Variants from dbSNP release 155
COVID GWAS v4 COVID risk variants from GWAS meta-analyses by the COVID-19 Host Genetics Initiative (Rel 4, Oct 2020)
COVID GWAS v3 GWAS meta-analyses from the COVID-19 Host Genetics Initiative
1000G Archive 1000 Genomes Archive
     1000G Ph3 Vars     1000 Genomes Phase 3 Integrated Variant Calls from IGSR: SNVs and Indels
     1000 Genomes Trios     Thousand Genomes Project Family VCF Trios
updated Array Probesets Microarray Probesets
dbSNP Archive dbSNP Track Archive
     All SNPs(141)     Simple Nucleotide Polymorphisms (dbSNP 141)
     Common SNPs(141)     Simple Nucleotide Polymorphisms (dbSNP 141) Found in >= 1% of Samples
     Flagged SNPs(141)     Simple Nucleotide Polymorphisms (dbSNP 141) Flagged by dbSNP as Clinically Assoc
     Mult. SNPs(141)     Simple Nucleotide Polymorphisms (dbSNP 141) That Map to Multiple Genomic Loci
     All SNPs(142)     Simple Nucleotide Polymorphisms (dbSNP 142)
     Common SNPs(142)     Simple Nucleotide Polymorphisms (dbSNP 142) Found in >= 1% of Samples
     Flagged SNPs(142)     Simple Nucleotide Polymorphisms (dbSNP 142) Flagged by dbSNP as Clinically Assoc
     Mult. SNPs(142)     Simple Nucleotide Polymorphisms (dbSNP 142) That Map to Multiple Genomic Loci
     All SNPs(144)     Simple Nucleotide Polymorphisms (dbSNP 144)
     Common SNPs(144)     Simple Nucleotide Polymorphisms (dbSNP 144) Found in >= 1% of Samples
     Flagged SNPs(144)     Simple Nucleotide Polymorphisms (dbSNP 144) Flagged by dbSNP as Clinically Assoc
     Mult. SNPs(144)     Simple Nucleotide Polymorphisms (dbSNP 144) That Map to Multiple Genomic Loci
     All SNPs(146)     Simple Nucleotide Polymorphisms (dbSNP 146)
     Common SNPs(146)     Simple Nucleotide Polymorphisms (dbSNP 146) Found in >= 1% of Samples
     Flagged SNPs(146)     Simple Nucleotide Polymorphisms (dbSNP 146) Flagged by dbSNP as Clinically Assoc
     Mult. SNPs(146)     Simple Nucleotide Polymorphisms (dbSNP 146) That Map to Multiple Genomic Loci
     All SNPs(147)     Simple Nucleotide Polymorphisms (dbSNP 147)
     Common SNPs(147)     Simple Nucleotide Polymorphisms (dbSNP 147) Found in >= 1% of Samples
     Flagged SNPs(147)     Simple Nucleotide Polymorphisms (dbSNP 147) Flagged by dbSNP as Clinically Assoc
     Mult. SNPs(147)     Simple Nucleotide Polymorphisms (dbSNP 147) That Map to Multiple Genomic Loci
     Flagged SNPs(150)     Simple Nucleotide Polymorphisms (dbSNP 150) Flagged by dbSNP as Clinically Assoc
     Common SNPs(150)     Simple Nucleotide Polymorphisms (dbSNP 150) Found in >= 1% of Samples
     All SNPs(150)     Simple Nucleotide Polymorphisms (dbSNP 150)
     Mult. SNPs(150)     Simple Nucleotide Polymorphisms (dbSNP 150) That Map to Multiple Genomic Loci
     Mult. SNPs(151)     Simple Nucleotide Polymorphisms (dbSNP 151) That Map to Multiple Genomic Loci
     Flagged SNPs(151)     Simple Nucleotide Polymorphisms (dbSNP 151) Flagged by dbSNP as Clinically Assoc
     All SNPs(151)     Simple Nucleotide Polymorphisms (dbSNP 151)
     Common SNPs(151)     Simple Nucleotide Polymorphisms (dbSNP 151) Found in >= 1% of Samples
     dbSNP 153     Short Genetic Variants from dbSNP release 153
dbVar Common Struct Var NCBI Curated Common Structural Variants from dbVar
     dbVar Conflict SV     NCBI dbVar Curated Conflict Variants
     dbVar Common SV     NCBI dbVar Curated Common Structural Variants
DGV Struct Var Database of Genomic Variants: Structural Variation (CNV, Inversion, In/del)
Genome In a Bottle Genome In a Bottle Structural Variants and Trios
gnomAD Variants Genome Aggregation Database (gnomAD) Genome and Exome Variants
     gnomAD Constraint Metrics     Genome Aggregation Database (gnomAD) Predicted Constraint Metrics (pLI and Z-scores)
     gnomAD Mut Constraint     Genome Aggregation Database (gnomAD) non-coding constraint of haploinsufficient variation (Gnocchi), includes chrX
     gnomAD v2     Genome Aggregation Database (gnomAD) Genome and Exome Variants v2.1
     gnomAD v3     Genome Aggregation Database (gnomAD) Genome Variants v3
     gnomAD v3.1.1     Genome Aggregation Database (gnomAD) Genome Variants v3.1.1
     gnomAD v3.1     Genome Aggregation Database (gnomAD) Genome Variants v3.1
     gnomAD v4 Pre-Release     Genome Aggregation Database (gnomAD) Genome Variants v4.0.0 Pre-Release
Platinum Genomes Platinum genome variants
-   Repeats    
RepeatMasker Repeating Elements by RepeatMasker
RepeatMasker #1 Repeating Elements by RepeatMasker (duplicate #1)
Interrupted Rpts Fragments of Interrupted Repeats Joined by RepeatMasker ID
Microsatellite Microsatellites - Di-nucleotide and Tri-nucleotide Repeats
Microsatellite #1 Microsatellites - Di-nucleotide and Tri-nucleotide Repeats (duplicate #1)
RepeatMasker Viz. Detailed Visualization of RepeatMasker Annotations
Segmental Dups Duplications of >1000 Bases of Non-RepeatMasked Sequence
Self Chain Human Chained Self Alignments
Self Chain chainSelf (duplicate #1)
Simple Repeats Simple Tandem Repeats by TRF
WM + SDust Genomic Intervals Masked by WindowMasker + SDust
WM + SDust windowmaskerSdust (duplicate #1)
WM + SDust #2 Genomic Intervals Masked by WindowMasker + SDust (duplicate #2)
WM + SDust #3 Genomic Intervals Masked by WindowMasker + SDust (duplicate #3)