Variant report

Variant rs2076006
Chromosome Location chr6:167707727-167707728
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167705800-167715000 Weak transcription Liver Liver
2 chr6:167706200-167718600 Weak transcription H9 Cell Line embryonic stem cell
3 chr6:167706400-167714600 Weak transcription H1 Cell Line embryonic stem cell
4 chr6:167706400-167717400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr6:167707000-167709400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr6:167707200-167707800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
7 chr6:167707200-167717600 Weak transcription Placenta Amnion Placenta Amnion
8 chr6:167707400-167708000 Enhancers HepG2 liver
9 chr6:167707400-167709600 Weak transcription Fetal Intestine Large intestine
10 chr6:167707400-167715400 Strong transcription Fetal Intestine Small intestine

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