Variant report

Variant rs9996956
Chromosome Location chr4:10464221-10464222
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:3 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:10462600-10465000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
2 chr4:10463600-10464400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr4:10463600-10465200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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