Variant report

Variant rs12909039
Chromosome Location chr15:31378480-31378481
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 chr15:31376400-31378600 Enhancers HepG2 liver
9 chr15:31377800-31378800 Enhancers Esophagus oesophagus
10 chr15:31378200-31379000 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin01 Skin
11 chr15:31378400-31378800 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr15:31378400-31378800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
13 chr15:31378400-31378800 Enhancers Lung lung
14 chr15:31378400-31379000 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin03 Skin

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