The 2.0 version of rSNPBase

Variant report

Variant rs2722177
Chromosome Location chr12:104438467-104438468
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:104408800-104442200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr12:104424800-104438800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr12:104428400-104439000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr12:104429600-104438800 Weak transcription Ovary ovary
5 chr12:104432800-104439000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr12:104435000-104442000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr12:104435400-104438800 Weak transcription Duodenum Smooth Muscle Duodenum
8 chr12:104435800-104441600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr12:104436000-104438800 Weak transcription Fetal Muscle Trunk muscle
10 chr12:104436400-104438800 Weak transcription Stomach Smooth Muscle stomach
11 chr12:104436600-104439000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr12:104436800-104439000 Weak transcription Fetal Stomach stomach
13 chr12:104436800-104440200 Weak transcription Aorta Aorta
14 chr12:104437600-104442000 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr12:104437800-104439600 Enhancers Fetal Muscle Leg muscle
16 chr12:104438000-104440600 Weak transcription Fetal Brain Female brain
17 chr12:104438400-104441800 Enhancers Colon Smooth Muscle Colon

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Last update: Aug 31, 2015