Variant report

Variant rs2054
Chromosome Location chr6:167717123-167717124
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167706200-167718600 Weak transcription H9 Cell Line embryonic stem cell
2 chr6:167706400-167717400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr6:167707200-167717600 Weak transcription Placenta Amnion Placenta Amnion
4 chr6:167711600-167718800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr6:167711600-167721600 Weak transcription Fetal Intestine Large intestine
6 chr6:167713600-167717600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr6:167714800-167718400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr6:167715000-167717800 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr6:167715000-167718400 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr6:167715400-167717200 Weak transcription Fetal Intestine Small intestine
11 chr6:167715400-167717600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr6:167715400-167717600 Enhancers HepG2 liver
13 chr6:167716200-167721200 Weak transcription Liver Liver
14 chr6:167716600-167719200 Enhancers ES-WA7 Cell Line embryonic stem cell

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