The 2.0 version of rSNPBase

Variant report

Variant rs59901009
Chromosome Location chr11:10178437-10178438
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr11:10177400-10178800 Enhancers Psoas Muscle Psoas
4 chr11:10177800-10183200 Weak transcription Ovary ovary
5 chr11:10177800-10183800 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr11:10178000-10182200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr11:10178000-10182200 Weak transcription HMEC breast
8 chr11:10178000-10183600 Weak transcription Right Ventricle heart
9 chr11:10178200-10180000 Weak transcription Hela-S3 cervix
10 chr11:10178200-10180400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr11:10178200-10180400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr11:10178200-10182200 Weak transcription NHLF lung
13 chr11:10178200-10182400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr11:10178200-10185400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr11:10178200-10213400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr11:10178400-10178600 Enhancers Pancreatic Islets Pancreatic Islet

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Last update: Aug 31, 2015