Variant report

Variant rs10167155
Chromosome Location chr2:110854766-110854767
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:110851400-110856400 Weak transcription Fetal Intestine Large intestine
2 chr2:110851800-110855400 Weak transcription Duodenum Mucosa Duodenum
3 chr2:110852600-110857200 Weak transcription Colonic Mucosa Colon
4 chr2:110852800-110858600 Genic enhancers A549 lung
5 chr2:110853200-110854800 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:110853200-110856400 Weak transcription HUVEC blood vessel
7 chr2:110853400-110854800 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:110853400-110854800 Weak transcription Fetal Lung lung
9 chr2:110853600-110855000 Weak transcription Stomach Mucosa stomach
10 chr2:110853600-110857800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:110853600-110858000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr2:110853600-110858000 Strong transcription Fetal Intestine Small intestine
13 chr2:110853600-110858000 Weak transcription NHLF lung
14 chr2:110854000-110856400 Weak transcription Lung lung
15 chr2:110854400-110855800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr2:110854600-110860600 Enhancers HMEC breast

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