Variant report

Variant rs114485801
Chromosome Location chr12:117087828-117087829
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:117080600-117088000 Weak transcription H9 Cell Line embryonic stem cell
2 chr12:117080600-117088000 Weak transcription Adipose Nuclei Adipose
3 chr12:117083200-117088200 Weak transcription Right Atrium heart
4 chr12:117084000-117088000 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr12:117084000-117088400 Weak transcription Lung lung
6 chr12:117084000-117093200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr12:117084200-117088000 Weak transcription H1 Cell Line embryonic stem cell
8 chr12:117084600-117088200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr12:117086600-117088000 Weak transcription Pancreas Pancrea
10 chr12:117086600-117088000 Weak transcription Dnd41 blood
11 chr12:117086800-117088200 Weak transcription Thymus Thymus
12 chr12:117087800-117088000 Bivalent/Poised TSS IMR90 fetal lung fibroblasts Cell Line lung
13 chr12:117087800-117088600 Enhancers Liver Liver
14 chr12:117087800-117089400 Enhancers Fetal Thymus thymus

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