Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:45634892-45635091 | Rare:53 | ||||
chr15:47717967-47718282 | Common:1; Rare:74 | ||||
chr15:47718382-47718624 | Common:1; Rare:60 | ||||
chr15:48330796-48331154 | Common:3; Rare:85 | ||||
chr15:48331353-48331472 | Rare:40 | ||||
chr15:48645663-48645879 | Common:2; Rare:69; Clinvar (benign):1 | ||||
chr15:48878017-48878338 | Rare:121 | ||||
chr15:49046280-49046605 | Common:2; Rare:122 | ||||
chr15:49155523-49155889 | Common:4; Rare:118 | ||||
chr15:49170124-49170318 | Rare:43 | ||||
chr15:49423111-49423404 | Common:1; Rare:49 | ||||
chr15:49620762-49621111 | Common:6; Rare:131 | ||||
chr15:49876503-49876588 | Rare:29 | ||||
chr15:50113300-50113499 | Common:1; Rare:36 | ||||
chr15:50354857-50355010 | Rare:25 |