Variant report

Variant rs9761396
Chromosome Location chr10:93209011-93209012
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr10:93205000-93211800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr10:93205800-93209200 Weak transcription Fetal Lung lung
9 chr10:93205800-93210800 Weak transcription Aorta Aorta
10 chr10:93208800-93209200 ZNF genes & repeats H1 Cell Line embryonic stem cell
11 chr10:93209000-93209600 ZNF genes & repeats Cortex derived primary cultured neurospheres brain

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