Variant report
| Variant | rs56976963 |
|---|---|
| Chromosome Location | chr8:49327594-49327595 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:49319800-49332400 | Weak transcription | Fetal Kidney | kidney |
| 2 | chr8:49322800-49329800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 3 | chr8:49323600-49330000 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 4 | chr8:49327400-49328000 | Strong transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
