Variant report
| Variant | rs2248721 |
|---|---|
| Chromosome Location | chr1:86915587-86915588 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:86897200-86922600 | Strong transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 2 | chr1:86897200-86922800 | Strong transcription | HMEC | breast |
| 3 | chr1:86897400-86916000 | Strong transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 4 | chr1:86903400-86926800 | Weak transcription | Esophagus | oesophagus |
| 5 | chr1:86913200-86915600 | Enhancers | K562 | blood |
| 6 | chr1:86914000-86915600 | Enhancers | Brain Substantia Nigra | brain |
| 7 | chr1:86914400-86917000 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 8 | chr1:86914600-86930800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 9 | chr1:86915200-86920000 | Strong transcription | NHEK | skin |
| 10 | chr1:86915400-86917400 | Enhancers | HUVEC | blood vessel |
