Variant report

Variant rs12081556
Chromosome Location chr1:162077722-162077723
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:162073000-162079600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr1:162074800-162084400 Weak transcription Gastric stomach
3 chr1:162076000-162080000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr1:162076200-162078200 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr1:162076600-162089200 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr1:162077200-162078400 Enhancers HepG2 liver
7 chr1:162077400-162077800 Enhancers Brain Cingulate Gyrus brain
8 chr1:162077400-162078000 Enhancers Brain Hippocampus Middle brain
9 chr1:162077400-162078400 Enhancers Brain Substantia Nigra brain
10 chr1:162077400-162080000 Enhancers Liver Liver
11 chr1:162077400-162080400 Strong transcription Cortex derived primary cultured neurospheres brain

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