The 2.0 version of rSNPBase

Variant report

Variant rs836628
Chromosome Location chr2:173501069-173501070
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173461400-173504200 Weak transcription NHEK skin
2 chr2:173462200-173507400 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr2:173472600-173504600 Weak transcription Adipose Nuclei Adipose
4 chr2:173474600-173504400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:173489200-173507200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr2:173489400-173504200 Weak transcription NHLF lung
7 chr2:173494600-173503800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr2:173494600-173504200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr2:173494600-173510200 Weak transcription Primary T cells from cord blood blood
10 chr2:173494800-173503800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr2:173494800-173504400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr2:173494800-173504400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr2:173499800-173513000 Weak transcription Pancreas Pancrea

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Last update: Aug 31, 2015