The 2.0 version of rSNPBase

Variant report

Variant rs2150269
Chromosome Location chr1:94709272-94709273
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94703600-94712000 Weak transcription HSMM muscle
2 chr1:94704800-94711400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr1:94705400-94709800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr1:94705800-94709800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr1:94705800-94709800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:94706000-94709800 Weak transcription Osteobl bone
7 chr1:94706400-94710000 Weak transcription A549 lung
8 chr1:94706600-94710400 Weak transcription NH-A brain
9 chr1:94708400-94710000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:94708600-94709400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:94708800-94709600 Enhancers HMEC breast
12 chr1:94708800-94709800 Weak transcription NHEK skin
13 chr1:94709000-94710200 Flanking Active TSS HUVEC blood vessel
14 chr1:94709000-94712200 Enhancers Liver Liver
15 chr1:94709200-94709800 ZNF genes & repeats HepG2 liver

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Last update: Aug 31, 2015