UCSC Genome Browser on Human (GRCh38/hg38)
Move Zoom in Zoom out
chr7:99,756,967-99,784,184 3,392 bp.
  
-   Custom Tracks
DMSO narrowPeak
eclipse_run1_bed
eclipse_run1_BedGraph
eclipse_run2_bed
eclipse_run2_BedGraph
eclipse_run3_bed
eclipse_run3_BedGraph
m6a_1
m6a_1_peaks
m6a_2
m6a_2_peaks
Previously studied PXR binding regions
prim_hep_kit_nogel_apr_bed
prim_hep_kit_nogel_apr_BedGraph
prim_hep_kit_run1_bed
prim_hep_kit_run1_BedGraph
prim_hep_kit_withgel_Jan2023_run2_bed
prim_hep_kit_withgel_Jan2023_run2_BedGraph
prim_hep_kit_withgel_Jan2023_run3_bed
prim_hep_kit_withgel_Jan2023_run3_BedGraph
RIF narrowPeak
+   Mapping and Sequencing
-   Genes and Gene Predictions
updated GENCODE V47
NCBI RefSeq
CCDS
CRISPR Targets
GENCODE Archive
updated GENCODE Versions
HGNC
IKMC Genes Mapped
LRG Transcripts
MANE
MGC/ORFeome Genes
Non-coding RNA
Old UCSC Genes
Other RefSeq
Pfam in GENCODE
Prediction Archive
RetroGenes V9
TransMap V5
UCSC Alt Events
UniProt
-   Phenotype and Literature
OMIM
AbSplice Scores
CADD 1.6
new CADD 1.7
Cancer Gene Expr
new ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COSMIC
COSMIC Regions
COVID Data
DECIPHER CNVs
DECIPHER SNVs
Development Delay
Dosage Sensitivity
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
HGMD public
LOVD Variants
Orphanet
PanelApp
REVEL Scores
SNPedia
new SpliceAI
TCGA Pan-Cancer
UniProt Variants
Variants in Papers
-   Human Pangenome - HPRC
Multiple Alignment
Pairwise Alignments
Rearrangements
Short Variants
+   mRNA and EST
+   Expression
-   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
Muscle De Micheli
Pancreas Baron
Placenta Vento-Tormo
Rectum Wang
Skin Sole-Boldo
Tabula Sapiens
-   Regulation
ENCODE cCREs
ENCODE Regulation
CpG Islands
FANTOM5
GeneHancer
GTEx cis-eQTLs
Hi-C and Micro-C
JASPAR Transcription Factors
ORegAnno
RefSeq Func Elems
ReMap ChIP-seq
VISTA Enhancers
+   Comparative Genomics
-   Variation
dbSNP 155
1000 Genomes
Array Probesets
dbSNP Archive
dbVar Common Struct Var
DGV Struct Var
Genome In a Bottle
new gnomAD Variants
Platinum Genomes
+   Repeats
Invisible link