Variant report
| Variant | rs1338769 |
|---|---|
| Chromosome Location | chr1:220546380-220546381 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:220542400-220552400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr1:220543600-220552000 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 3 | chr1:220544400-220547200 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 4 | chr1:220544800-220548000 | Weak transcription | Psoas Muscle | Psoas |
| 5 | chr1:220545000-220552000 | Weak transcription | Hela-S3 | cervix |
| 6 | chr1:220545200-220548000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 7 | chr1:220546200-220546400 | Enhancers | Esophagus | oesophagus |
