Variant report

Variant rs12917436
Chromosome Location chr15:31382402-31382403
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:31376200-31383200 Weak transcription Pancreas Pancrea
2 chr15:31376200-31384800 Weak transcription Gastric stomach
3 chr15:31376200-31389000 Weak transcription Right Atrium heart
4 chr15:31376200-31390800 Weak transcription Brain Substantia Nigra brain
5 chr15:31378800-31383400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr15:31379800-31388600 Weak transcription Placenta Placenta
7 chr15:31380600-31383000 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin03 Skin
8 chr15:31382200-31383400 Weak transcription Esophagus oesophagus
9 chr15:31382200-31383600 Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
10 chr15:31382200-31385800 Enhancers HepG2 liver

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