Variant report
| Variant | rs58279400 |
|---|---|
| Chromosome Location | chr1:86922993-86922994 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:86903400-86926800 | Weak transcription | Esophagus | oesophagus |
| 2 | chr1:86914600-86930800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 3 | chr1:86917000-86930600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 4 | chr1:86920000-86924000 | Weak transcription | NHEK | skin |
| 5 | chr1:86920800-86923400 | Enhancers | K562 | blood |
| 6 | chr1:86921600-86925400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 7 | chr1:86922600-86930800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 8 | chr1:86922800-86924800 | Weak transcription | HMEC | breast |
