Variant report

Variant rs12909383
Chromosome Location chr15:31378667-31378668
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:31373400-31379000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr15:31375800-31379200 Weak transcription Placenta Placenta
3 chr15:31376200-31379200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr15:31376200-31383200 Weak transcription Pancreas Pancrea
5 chr15:31376200-31384800 Weak transcription Gastric stomach
6 chr15:31376200-31389000 Weak transcription Right Atrium heart
7 chr15:31376200-31390800 Weak transcription Brain Substantia Nigra brain
8 chr15:31377800-31378800 Enhancers Esophagus oesophagus
9 chr15:31378200-31379000 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin01 Skin
10 chr15:31378400-31378800 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr15:31378400-31378800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
12 chr15:31378400-31378800 Enhancers Lung lung
13 chr15:31378400-31379000 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin03 Skin
14 chr15:31378600-31379600 Weak transcription HepG2 liver

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