Variant report

Variant rs11186573
Chromosome Location chr10:93212975-93212976
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:93184400-93226400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr10:93186000-93226800 Weak transcription Pancreas Pancrea
3 chr10:93194600-93213800 Weak transcription HUVEC blood vessel
4 chr10:93195600-93213000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr10:93196000-93220600 Weak transcription Hela-S3 cervix
6 chr10:93210800-93214200 ZNF genes & repeats Fetal Lung lung
7 chr10:93210800-93214400 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
8 chr10:93211200-93213000 Weak transcription Aorta Aorta
9 chr10:93211800-93213400 ZNF genes & repeats Psoas Muscle Psoas
10 chr10:93211800-93213600 ZNF genes & repeats Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr10:93212400-93214200 ZNF genes & repeats Adipose Nuclei Adipose
12 chr10:93212600-93214400 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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