Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:45147753-45147891 | Rare:28 | ||||
chr15:45151494-45151801 | Common:1; Rare:61 | ||||
chr15:45152052-45152344 | Common:3; Rare:86 | ||||
chr15:45378384-45378678 | Common:4; Rare:87; Clinvar:3; Clinvar (benign):11 | ||||
chr15:45587296-45587470 | Rare:52; Clinvar:6 | ||||
chr15:45634898-45635107 | Common:1; Rare:56 | ||||
chr15:47717158-47717561 | Common:1; Rare:83 | ||||
chr15:48331381-48331476 | Rare:31 | ||||
chr15:48878059-48878618 | Common:1; Rare:205 | ||||
chr15:49046371-49046614 | Common:2; Rare:85 | ||||
chr15:49155513-49155877 | Common:2; Rare:116 | ||||
chr15:49170101-49170315 | Rare:48 | ||||
chr15:49423111-49423262 | Common:1; Rare:30 | ||||
chr15:49620806-49621099 | Common:6; Rare:115 | ||||
chr15:50354862-50354987 | Rare:18 |