Variant report
| Variant | rs72855277 |
|---|---|
| Chromosome Location | chr2:31236026-31236027 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:31232600-31251000 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 2 | chr2:31234400-31236400 | Enhancers | NHEK | skin |
| 3 | chr2:31234600-31236400 | Enhancers | HMEC | breast |
| 4 | chr2:31234800-31236400 | Enhancers | H1 Cell Line | embryonic stem cell |
| 5 | chr2:31235200-31236600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 6 | chr2:31235200-31236800 | Flanking Active TSS | Primary neutrophils fromperipheralblood | blood |
| 7 | chr2:31235200-31251000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 8 | chr2:31235400-31236400 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 9 | chr2:31235400-31251000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 10 | chr2:31236000-31236400 | Active TSS | Primary B cells from cord blood | blood |
