UCSC Genome Browser on Human (GRCh38/hg38)
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chr9:33,241,160-33,348,013 106,854 bp.
  
-   Custom Tracks
RS4-WDR5
RS4-WDR5_control
RS4-WDR5_broad_control
RS4-WDR5_broad
RS4-H3K4me3_control
RS4-H3K4me3
RS4-H3K4me3_broad_control
RS4-H3K4me3_broad
-   Mapping and Sequencing
Base Position
p14 Fix Patches
p14 Alt Haplotypes
Assembly
Assembly Tracks
Centromeres
Chromosome Band
Clone Ends
Exome Probesets
Gap
GC Percent
GRC Incident
Hg19 Diff
INSDC
LiftOver & ReMap
LRG Regions
Mappability
updated Problematic Regions
Recomb Rate
RefSeq Acc
Restr Enzymes
Short Match
-   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
-   Human Pangenome - HPRC
Multiple Alignment
Pairwise Alignments
Rearrangements
Short Variants
+   mRNA and EST
+   Expression
+   Single Cell RNA-seq
-   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
RepeatMasker
Interrupted Rpts
Microsatellite
NuMTs Sequence
RepeatMasker Viz.
Segmental Dups
Self Alignment
Simple Repeats
WM + SDust
Invisible link