The 2.0 version of rSNPBase

Variant report

Variant rs73159522
Chromosome Location chr7:98904530-98904531
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:98873200-98905800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:98874800-98906800 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr7:98890800-98905800 Weak transcription Pancreas Pancrea
4 chr7:98893200-98906600 Weak transcription Fetal Intestine Small intestine
5 chr7:98893800-98906000 Weak transcription HMEC breast
6 chr7:98899200-98907800 Weak transcription Aorta Aorta
7 chr7:98899400-98907000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr7:98899400-98907200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr7:98903800-98910400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr7:98904000-98907400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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Last update: Aug 31, 2015