Variant report
Variant | rs1894692 |
---|---|
Chromosome Location | chr1:169467654-169467655 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:169465200-169468000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
2 | chr1:169465600-169468600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
3 | chr1:169465800-169468800 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
4 | chr1:169467000-169467800 | Enhancers | Placenta Amnion | Placenta Amnion |
5 | chr1:169467000-169469000 | Enhancers | Placenta | Placenta |
6 | chr1:169467400-169467800 | Weak transcription | HepG2 | liver |
7 | chr1:169467400-169468000 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
8 | chr1:169467600-169467800 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |