The 2.0 version of rSNPBase

Variant report

Variant rs17308922
Chromosome Location chr11:26254003-26254004
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26250200-26256000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr11:26251800-26259200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:26252800-26255600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:26253400-26256000 Weak transcription Hela-S3 cervix
5 chr11:26253800-26255600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr11:26253800-26255800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:26253800-26256000 Weak transcription Muscle Satellite Cultured Cells --
8 chr11:26254000-26255800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr11:26254000-26255800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr11:26254000-26255800 Weak transcription HUVEC blood vessel
11 chr11:26254000-26255800 Weak transcription NHEK skin
12 chr11:26254000-26256000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr11:26254000-26256000 Weak transcription NHDF-Ad bronchial
14 chr11:26254000-26256200 Weak transcription HMEC breast

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Last update: Aug 31, 2015