Variant report

Variant rs13198547
Chromosome Location chr6:167718396-167718397
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr6:167717600-167719000 Weak transcription HepG2 liver
10 chr6:167717600-167720400 Enhancers Placenta Amnion Placenta Amnion
11 chr6:167717800-167718400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr6:167717800-167718600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr6:167717800-167719800 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr6:167717800-167724000 Weak transcription Fetal Brain Female brain
15 chr6:167718000-167719200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr6:167718000-167719400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links