Variant report

Variant rs72578735
Chromosome Location chr6:167810309-167810310
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167807600-167814400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:167809200-167812600 Enhancers Liver Liver
3 chr6:167809200-167812800 Enhancers Fetal Intestine Small intestine
4 chr6:167809400-167811800 Enhancers Stomach Mucosa stomach
5 chr6:167809400-167812800 Enhancers Fetal Intestine Large intestine
6 chr6:167809600-167810400 Flanking Bivalent TSS/Enh HepG2 liver
7 chr6:167809800-167810400 Weak transcription Fetal Lung lung
8 chr6:167809800-167810400 Enhancers Rectal Mucosa Donor 31 rectum
9 chr6:167810000-167810600 Enhancers Pancreas Pancrea
10 chr6:167810000-167811400 Enhancers Gastric stomach

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