Variant report

Variant rs11070808
Chromosome Location chr15:31390533-31390534
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:31376200-31390800 Weak transcription Brain Substantia Nigra brain
2 chr15:31385600-31390800 Weak transcription Stomach Mucosa stomach
3 chr15:31385600-31390800 Weak transcription A549 lung
4 chr15:31386000-31392400 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin03 Skin
5 chr15:31388800-31390800 Weak transcription Placenta Placenta
6 chr15:31388800-31391400 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin01 Skin
7 chr15:31389200-31391600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr15:31389200-31393000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr15:31389600-31390800 Enhancers Fetal Kidney kidney
10 chr15:31389600-31393200 Enhancers Liver Liver
11 chr15:31389800-31392200 Enhancers HepG2 liver
12 chr15:31390000-31390800 Weak transcription Esophagus oesophagus
13 chr15:31390000-31391200 Weak transcription ES-I3 Cell Line embryonic stem cell

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