The 2.0 version of rSNPBase

Variant report

Variant rs56319831
Chromosome Location chr11:10179849-10179850
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10170600-10189000 Weak transcription Left Ventricle heart
2 chr11:10176200-10184000 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr11:10177800-10183200 Weak transcription Ovary ovary
4 chr11:10177800-10183800 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr11:10178000-10182200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:10178000-10182200 Weak transcription HMEC breast
7 chr11:10178000-10183600 Weak transcription Right Ventricle heart
8 chr11:10178200-10180000 Weak transcription Hela-S3 cervix
9 chr11:10178200-10180400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr11:10178200-10180400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr11:10178200-10182200 Weak transcription NHLF lung
12 chr11:10178200-10182400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr11:10178200-10185400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr11:10178200-10213400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
15 chr11:10179800-10181200 Enhancers Muscle Satellite Cultured Cells --

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Last update: Aug 31, 2015