Variant report
| Variant | rs10107935 |
|---|---|
| Chromosome Location | chr8:126502336-126502337 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:126496600-126503000 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 2 | chr8:126498600-126509200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 3 | chr8:126498600-126509800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 4 | chr8:126499000-126503200 | Weak transcription | Primary B cells from cord blood | blood |
| 5 | chr8:126499400-126503000 | Weak transcription | Placenta | Placenta |
| 6 | chr8:126501600-126502400 | Enhancers | NHEK | skin |
| 7 | chr8:126502000-126502400 | Enhancers | Primary T helper 17 cells PMA-I stimulated | -- |
| 8 | chr8:126502000-126502600 | Enhancers | Primary hematopoietic stem cells | blood |
| 9 | chr8:126502200-126502600 | Flanking Active TSS | Liver | Liver |
| 10 | chr8:126502200-126503000 | Weak transcription | Adipose Nuclei | Adipose |
| 11 | chr8:126502200-126503400 | Enhancers | HepG2 | liver |
| 12 | chr8:126502200-126509800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
