Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:48331359-48331472 | Rare:39 | ||||
chr15:48645710-48645903 | Common:2; Rare:63; Clinvar (benign):1 | ||||
chr15:48878043-48878619 | Common:1; Rare:209 | ||||
chr15:49155562-49155869 | Common:2; Rare:104 | ||||
chr15:49170124-49170298 | Rare:38 | ||||
chr15:49423111-49423418 | Common:1; Rare:51 | ||||
chr15:49620714-49621099 | Common:7; Rare:134 | ||||
chr15:50354669-50354998 | Common:1; Rare:103 | ||||
chr15:50355093-50355534 | Common:3; Rare:186 | ||||
chr15:50424129-50424500 | Common:2; Rare:130 | ||||
chr15:50686704-50686914 | Common:4; Rare:87 | ||||
chr15:50765536-50765809 | Common:2; Rare:96 | ||||
chr15:50908595-50908781 | Common:1; Rare:80; Clinvar (benign):3 | ||||
chr15:51751512-51751688 | Common:1; Rare:45 | ||||
chr15:51971732-51971841 | Rare:51 |