Variant report

Variant rs1033017
Chromosome Location chr2:110853221-110853222
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:110847200-110853600 Weak transcription Fetal Intestine Small intestine
2 chr2:110851400-110856400 Weak transcription Fetal Intestine Large intestine
3 chr2:110851800-110853400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:110851800-110855400 Weak transcription Duodenum Mucosa Duodenum
5 chr2:110852600-110853400 Enhancers Fetal Lung lung
6 chr2:110852600-110853600 Enhancers Stomach Mucosa stomach
7 chr2:110852600-110857200 Weak transcription Colonic Mucosa Colon
8 chr2:110852800-110853600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr2:110852800-110854600 Weak transcription HMEC breast
10 chr2:110852800-110858600 Genic enhancers A549 lung
11 chr2:110853200-110853600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr2:110853200-110853600 Enhancers NHLF lung
13 chr2:110853200-110854800 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr2:110853200-110856400 Weak transcription HUVEC blood vessel

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