Variant report

Variant rs12263089
Chromosome Location chr10:93212246-93212247
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:93176600-93212600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr10:93184400-93226400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr10:93186000-93226800 Weak transcription Pancreas Pancrea
4 chr10:93194600-93213800 Weak transcription HUVEC blood vessel
5 chr10:93195600-93213000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr10:93196000-93220600 Weak transcription Hela-S3 cervix
7 chr10:93210800-93214200 ZNF genes & repeats Fetal Lung lung
8 chr10:93210800-93214400 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
9 chr10:93211200-93213000 Weak transcription Aorta Aorta
10 chr10:93211800-93213400 ZNF genes & repeats Psoas Muscle Psoas
11 chr10:93211800-93213600 ZNF genes & repeats Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr10:93212000-93212600 ZNF genes & repeats Liver Liver
13 chr10:93212200-93212400 ZNF genes & repeats Colon Smooth Muscle Colon

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