The 2.0 version of rSNPBase

Variant report

Variant rs10188207
Chromosome Location chr2:173536088-173536089
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173521400-173536800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:173530400-173536400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:173530600-173536400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:173530800-173536400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:173532400-173536400 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr2:173533000-173536800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr2:173533200-173536400 Weak transcription Muscle Satellite Cultured Cells --
8 chr2:173533400-173536400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr2:173533400-173536400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr2:173533400-173536400 Weak transcription NHDF-Ad bronchial
11 chr2:173533400-173536600 Weak transcription Osteobl bone
12 chr2:173533400-173537000 Weak transcription NHLF lung
13 chr2:173533400-173537600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr2:173535000-173537000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr2:173535600-173536400 Enhancers A549 lung
16 chr2:173535800-173536800 Weak transcription Duodenum Mucosa Duodenum
17 chr2:173536000-173536400 Weak transcription Fetal Intestine Small intestine

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Last update: Aug 31, 2015