Variant report

Variant rs56362747
Chromosome Location chr6:167710745-167710746
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr6:167707200-167717600 Weak transcription Placenta Amnion Placenta Amnion
6 chr6:167707400-167715400 Strong transcription Fetal Intestine Small intestine
7 chr6:167707800-167711400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr6:167709600-167710800 Strong transcription Fetal Intestine Large intestine
9 chr6:167709600-167711200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr6:167709800-167710800 Strong transcription HepG2 liver
11 chr6:167710400-167711400 Enhancers Fetal Thymus thymus

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