Variant report
| Variant | rs17481440 |
|---|---|
| Chromosome Location | chr1:71334086-71334087 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:71330800-71343200 | Weak transcription | K562 | blood |
| 2 | chr1:71331400-71334800 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
| 3 | chr1:71331600-71337200 | Weak transcription | Fetal Heart | heart |
| 4 | chr1:71332800-71336600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
| 5 | chr1:71332800-71337000 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 6 | chr1:71332800-71338800 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 7 | chr1:71333000-71334400 | Enhancers | Primary T cells from cord blood | blood |
