The 2.0 version of rSNPBase

Variant report

Variant rs11673955
Chromosome Location chr2:21134892-21134893
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:21130000-21135800 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr2:21131200-21136400 Enhancers Fetal Adrenal Gland Adrenal Gland
3 chr2:21131600-21136400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr2:21131600-21136600 Weak transcription NHEK skin
5 chr2:21131800-21137000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:21133000-21135200 Enhancers Colon Smooth Muscle Colon
7 chr2:21133000-21135200 Enhancers Rectal Smooth Muscle rectum
8 chr2:21133000-21136400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:21133400-21136800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr2:21133400-21149400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr2:21134400-21135200 Enhancers Gastric stomach
12 chr2:21134400-21135600 Enhancers Ovary ovary
13 chr2:21134400-21135600 Enhancers Stomach Mucosa stomach
14 chr2:21134600-21135200 Enhancers Fetal Muscle Trunk muscle
15 chr2:21134800-21135600 Bivalent Enhancer HepG2 liver

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Last update: Aug 31, 2015