Skip to main content UCSC Genome Browser on Human (GRCh38/hg38)
Move Zoom in Zoom out
chr9:133,255,176-133,275,214 20,039 bp.
  
-   Visible Tracks  
Chromosome Band
p14 GRC Patches
Problematic Regions
NCBI RefSeq
MANE
COVID Data
dbSNP 155
GTEx Gene V8
ENCODE cCREs
new ENCODE4 Regulation
UCSC 100 Vertebrates
RepeatMasker
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Hub:  
Track hub error : Non-numeric port name
-   Mapping and Sequencing  
Base Position
Assembly
Assembly Tracks
Centromeres
Chromosome Band
Clone Ends
Exome Probesets
Gap
GC Percent
GRC Incident
p14 GRC Patches
Hg19 Diff
INSDC
LiftOver & ReMap
LRG Regions
Mappability
Problematic Regions
Recomb Rate
RefSeq Acc
Restr Enzymes
Short Match
-   Genes and Gene Predictions  
NCBI RefSeq
CCDS
CRISPR Targets
GENCODE Archive
GENCODE Versions
HGNC
IKMC Genes Mapped
LRG Transcripts
MANE
MGC/ORFeome Genes
new NMD Escape
Non-canonical ORFs
Non-coding RNA
Other RefSeq
Pfam in GENCODE
Prediction Archive
Pseudogenes
RetroGenes V9
TransMap V5
UCSC Alt Events
UniProt
-   Phenotypes, Variants, and Literature  
AlphaMissense
CADD 1.6
CADD 1.7
Cancer Gene Expr
CIViC
ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COVID Data
updated Deleteriousness Predictions
Development Delay
Dosage Sensitivity
G2P Project
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
MITOMAP
[No data-chr9]
Orphanet
PanelApp
REVEL Scores
SNPedia
Splicing Impact
TCGA Pan-Cancer
UniProt Variants
updated Variants in Papers
-   Variation  
dbSNP 155
1000 Genomes
Ancient Hominids
Array Probesets
dbSNP Archive
dbVar Struct Var
DGV Struct Var
Genome In a Bottle
new gnomAD
new Long-read SVs
Phased Variants
Platinum Genomes
new Tandem Repeat Variation
-   Human Pangenome - HPRC  
Multiple Alignment
Pairwise Alignments
Rearrangements
Short Variants
-   RNA and Transcriptome  
Human ESTs
Human mRNAs
Long-read Transcripts
Other ESTs
Other mRNAs
recount3
SIB Alt-Splicing
Spliced ESTs
-   Expression  
GTEx Gene V8
GTEx RNA-Seq Coverage
Affy Archive
EPDnew Promoters
GNF Atlas 2
GTEx Gene
GTEx Transcript
GWIPS-viz Riboseq
MaveDB Experiments
miRNA Tissue Atlas
Single Cell Expression
+   Single Cell RNA-seq  
-   Regulation  
ENCODE cCREs
new ENCODE4 Regulation
ENCODE3 Regulation
DNA Methylation
CpG Islands
FANTOM5
GTEx cis-eQTLs
Hi-C and Micro-C
JASPAR Transcription Factors
new MPRAs
ORegAnno
RefSeq Func Elems
ReMap ChIP-seq
VISTA Enhancers
-   Comparative Genomics  
UCSC 100 Vertebrates
Zoonomia 241 Placent
UCSC 30 Primates
Primate Chain/Net
Placental Chain/Net
Vertebrate Chain/Net
CHM13 alignments
Hiller Lab 470 Mammals
Unusually Conserved
Zoonomia+Primates 447
-   Repeats  
RepeatMasker
Interrupted Rpts
Microsatellite
NuMTs Sequence
RepeatMasker Viz.
Segmental Dups
Self Alignment
Simple Repeats
WM + SDust
Invisible link