Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:45114105-45114327 | Common:2; Rare:46 | ||||
chr15:45129842-45130023 | Rare:39 | ||||
chr15:45150447-45150701 | Common:3; Rare:58 | ||||
chr15:45378481-45378716 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):4 | ||||
chr15:45587300-45587474 | Rare:52; Clinvar:6 | ||||
chr15:45634671-45634779 | Rare:27 | ||||
chr15:45634916-45635084 | Rare:45 | ||||
chr15:48331253-48331472 | Common:4; Rare:70 | ||||
chr15:48645691-48645893 | Common:2; Rare:65; Clinvar (benign):1 | ||||
chr15:48877995-48878362 | Rare:137 | ||||
chr15:49155528-49155870 | Common:2; Rare:114 | ||||
chr15:49620806-49621099 | Common:6; Rare:115 | ||||
chr15:50119220-50119396 | Rare:26 | ||||
chr15:50354703-50354967 | Rare:81 | ||||
chr15:50355106-50355513 | Common:3; Rare:164 |