The 2.0 version of rSNPBase

Variant report

Variant rs4756099
Chromosome Location chr11:34052493-34052494
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:34050000-34052600 Enhancers NHEK skin
2 chr11:34050400-34055800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr11:34050600-34057800 Weak transcription Fetal Intestine Large intestine
4 chr11:34051000-34052600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr11:34051000-34053000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr11:34051000-34053200 Enhancers Placenta Placenta
7 chr11:34051400-34053400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr11:34051600-34053000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:34052200-34055600 Weak transcription HMEC breast
10 chr11:34052400-34052600 ZNF genes & repeats ES-WA7 Cell Line embryonic stem cell

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Last update: Aug 31, 2015