UCSC Genome Browser on Human Feb. 2009 (GRCh37/hg19) Assembly
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chrX:37,305,265-129,056,049 91,750,785 bp.
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-   Custom Tracks
GSM733660_hg19_wgEncodeBroadHistoneHmecH3k27acStdSig
Breast Luminal H3K27m3
FANTOM5_Promoter_Level_Expression
MCF-7 CTCF binding sites_GSE30263
MCF7 H3K27Ac Ins_Su 2015
MCF7_H3K27AC
MDA231 H3K27 Ac INS Su2015
Transcript Start Clusters_SwissRegulon
-   Mapping and Sequencing
Base Position
Fix Patches
Alt Haplotypes
Assembly
BAC End Pairs
BU ORChID
Chromosome Band
deCODE Recomb
[No data-chrX]
ENCODE Pilot
Exome Probesets
FISH Clones
Fosmid End Pairs
Gap
GC Percent
GRC Incident
GRC Map Contigs
Hg18 Diff
Hg38 Diff
Hg38 Mapping
Hi Seq Depth
INSDC
LRG Regions
Map Contigs
Mappability
Problematic Regions
Recomb Rate
RefSeq Acc
Restr Enzymes
Short Match
STS Markers
-   Genes and Gene Predictions
UCSC Genes
NCBI RefSeq
CCDS
CRISPR Targets
updated Ensembl Genes
EvoFold
Exoniphy
updated GENCODE
H-Inv 7.0
IKMC Genes Mapped
lincRNAs
LRG Transcripts
MGC Genes
Old UCSC Genes
ORFeome Clones
Other RefSeq
Pfam in UCSC Gene
new Prediction Archive
Retroposed Genes
sno/miRNA
TransMap V5
tRNA Genes
UCSC Alt Events
UniProt
Vega Genes
Yale Pseudo60
-   Phenotype and Literature
Publications
CADD
ClinGen
deprecated ClinGen CNVs
ClinVar Variants
Coriell CNVs
COSMIC Regions
Decipher CNVs
DECIPHER SNVs
Development Delay
GAD View
Gene Interactions
GeneReviews
GWAS Catalog
Haploinsufficiency
HGMD Variants
Lens Patents
LOVD Variants
MGI Mouse QTL
OMIM Alleles
OMIM Cyto Loci
OMIM Genes
new REVEL Scores
RGD Human QTL
RGD Rat QTL
SNPedia
UniProt Variants
Variants in Papers
Web Sequences
-   COVID-19
COVID GWAS v4
[No data-chrX]
COVID GWAS v3
[No data-chrX]
Rare Harmful Vars
-   mRNA and EST
CGAP SAGE
Gene Bounds
H-Inv
Human ESTs
Human mRNAs
Human RNA Editing
Ot