Variant report

Variant rs12491495
Chromosome Location chr3:499695-499696
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:492000-504600 Weak transcription Aorta Aorta
2 chr3:493000-500400 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr3:493200-500400 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr3:494200-500600 Weak transcription H1 Cell Line embryonic stem cell
5 chr3:497600-500400 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr3:497800-500000 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr3:497800-500600 Weak transcription Fetal Intestine Large intestine
8 chr3:498000-500400 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr3:498200-500400 Weak transcription Fetal Intestine Small intestine
10 chr3:499200-499800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr3:499200-500400 Enhancers Fetal Brain Male brain
12 chr3:499400-499800 Enhancers Brain Germinal Matrix brain
13 chr3:499600-500200 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr3:499600-500200 Active TSS Ovary ovary
15 chr3:499600-504400 Weak transcription Psoas Muscle Psoas

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