Variant report
| Variant | rs59901477 |
|---|---|
| Chromosome Location | chr13:37665316-37665317 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:37660400-37666600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 2 | chr13:37663400-37665400 | Weak transcription | Primary hematopoietic stem cells | blood |
| 3 | chr13:37664400-37667400 | Flanking Active TSS | Primary neutrophils fromperipheralblood | blood |
| 4 | chr13:37664600-37665400 | Flanking Active TSS | Monocytes-CD14+_RO01746 | blood |
| 5 | chr13:37665000-37665400 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 6 | chr13:37665000-37668200 | Active TSS | Primary B cells from cord blood | blood |
| 7 | chr13:37665200-37665400 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 8 | chr13:37665200-37665400 | Enhancers | Spleen | Spleen |
| 9 | chr13:37665200-37666600 | Enhancers | Fetal Muscle Leg | muscle |
