Variant report
Variant | rs17737261 |
---|---|
Chromosome Location | chr10:25983573-25983574 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:25962800-25993600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr10:25978400-25985600 | Enhancers | Primary B cells from peripheral blood | blood |
3 | chr10:25980200-25985600 | Enhancers | Primary Natural Killer cells fromperipheralblood | blood |
4 | chr10:25980800-25985200 | Enhancers | Primary B cells from cord blood | blood |
5 | chr10:25980800-25990000 | Weak transcription | H9 Cell Line | embryonic stem cell |
6 | chr10:25981800-25983600 | Weak transcription | Primary hematopoietic stem cells | blood |
7 | chr10:25983200-25983800 | Enhancers | Placenta | Placenta |
8 | chr10:25983200-25984400 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
9 | chr10:25983400-25984400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |