UCSC Genome Browser on Human (GRCh38/hg38)
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chr7:150,944,961-150,978,321 4,881 bp.
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-   Custom Tracks
DMSO narrowPeak
eCLIPSE_run1_bed
eCLIPSE_run1_BedGraph
eCLIPSE_run2_bed
eCLIPSE_run2_BedGraph
hepG2_kit1_bed
hepG2_kit1_BedGraph
let7_bed
let7_BedGraph
mir122_bed
mir122_BedGraph
mir125b_bed
mir125b_BedGraph
mir1275_bed
mir1275_BedGraph
mir148a_bed
mir148a_BedGraph
mir192_bed
mir192_BedGraph
mir27b_bed
mir27b_BedGraph
mir320a_bed
mir320a_BedGraph
mir34a_bed
mir34a_BedGraph
overholser_run1_bed
overholser_run1_BedGraph
Previously studied PXR binding regions
qCLASH_hela_bed
qCLASH_hela_BedGraph
qCLASH_prim_hep_23Mcells_bed
qCLASH_prim_hep_23Mcells_BedGraph
qCLASH_prim_hep_32Mcells_bed
qCLASH_prim_hep_32Mcells_BedGraph
qCLASH_prim_hep_9Mcells_bed
qCLASH_prim_hep_9Mcells_BedGraph
RIF narrowPeak
+   Mapping and Sequencing
-   Genes and Gene Predictions
GENCODE V44
NCBI RefSeq
CCDS
CRISPR Targets
updated GENCODE Versions
HGNC
IKMC Genes Mapped
LRG Transcripts
MANE
MGC Genes
Non-coding RNA
Old UCSC Genes
ORFeome Clones
Other RefSeq
Pfam in GENCODE
Prediction Archive
RetroGenes V9
TransMap V5
UCSC Alt Events
UniProt
-   Phenotype and Literature
OMIM Alleles
COVID Rare Harmful Var
new AbSplice Scores
CADD
Cancer Gene Expr
ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COSMIC
COSMIC Regions
DECIPHER CNVs
DECIPHER SNVs
Development Delay
new Dosage Sensitivity
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
HGMD public
LOVD Variants
OMIM Cyto Loci
OMIM Genes
Orphanet
PanelApp
REVEL Scores
SNPedia
TCGA Pan-Cancer
UniProt Variants
updated Variants in Papers
-   Human Pangenome - HPRC
new Multiple Alignment
new Pairwise Alignments
new Rearrangements
new Short Variants
-   Single Cell RNA-seq
Blood (PBMC) Hao
Colon Wang
Cortex Velmeshev
Cross Tissue Nuclei
Fetal Gene Atlas
Heart Cell Atlas
Ileum Wang
Kidney Stewart
Liver MacParland
Lung Travaglini
Merged Cells
Muscle De Micheli
Pancreas Baron
Placenta Vento-Tormo
Rectum Wang
Skin Sole-Boldo
Tabula Sapiens
+   mRNA and EST
+   Expression
-   Regulation
ENCODE cCREs
ENCODE Regulation
CpG Islands
new FANTOM5
GeneHancer
GTEx cis-eQTLs
Hi-C and Micro-C
updated JASPAR Transcription Factors
ORegAnno
RefSeq Func Elems
ReMap ChIP-seq
VISTA Enhancers
+   Comparative Genomics
-   Variation
dbSNP 155
COVID GWAS v4
COVID GWAS v3
1000G Archive
updated Array Probesets
dbSNP Archive
dbVar Common Struct Var
DGV Struct Var
Genome In a Bottle
gnomAD Variants
Platinum Genomes
+   Repeats
Invisible link