Variant report

Variant rs2072762
Chromosome Location chr6:167717854-167717855
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr6:167711600-167718800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr6:167711600-167721600 Weak transcription Fetal Intestine Large intestine
4 chr6:167714800-167718400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr6:167715000-167718400 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr6:167716200-167721200 Weak transcription Liver Liver
7 chr6:167716600-167719200 Enhancers ES-WA7 Cell Line embryonic stem cell
8 chr6:167717200-167721800 Strong transcription Fetal Intestine Small intestine
9 chr6:167717400-167718000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr6:167717400-167718000 Bivalent Enhancer Fetal Muscle Trunk muscle
11 chr6:167717600-167718000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr6:167717600-167719000 Weak transcription HepG2 liver
13 chr6:167717600-167720400 Enhancers Placenta Amnion Placenta Amnion
14 chr6:167717800-167718400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr6:167717800-167718600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr6:167717800-167719800 Enhancers iPS-18 Cell Line embryonic stem cell
17 chr6:167717800-167724000 Weak transcription Fetal Brain Female brain

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