UCSC Genome Browser on Human (GRCh38/hg38)
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chr7:99,756,967-99,784,184 3,392 bp.
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-   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
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
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
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