Variant report

Variant rs2003656
Chromosome Location chr6:167712298-167712299
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr6:167710800-167715400 Weak transcription HepG2 liver
8 chr6:167711400-167713600 Weak transcription Fetal Thymus thymus
9 chr6:167711600-167713000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr6:167711600-167718800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr6:167711600-167721600 Weak transcription Fetal Intestine Large intestine
12 chr6:167711800-167712800 Weak transcription Thymus Thymus

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