| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40470907-40471067 | Rare:53 | ||||
| chr15:40471341-40471389 | Common:1; Rare:17; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr15:40564559-40564672 | Rare:21 | ||||
| chr15:40564834-40564913 | Rare:13 | ||||
| chr15:40564949-40565280 | Common:3; Rare:65 | ||||
| chr15:40569169-40569607 | Common:3; Rare:136 | ||||
| chr15:40569834-40569956 | Common:2; Rare:32 | ||||
| chr15:40593863-40594065 | Common:1; Rare:105 | ||||
| chr15:40594194-40594381 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr15:40594495-40594730 | Common:3; Rare:68 | ||||
| chr15:40694507-40694824 | Rare:86 | ||||
| chr15:40694911-40695243 | Common:2; Rare:99 | ||||
| chr15:40695478-40695581 | Common:2; Rare:30 | ||||
| chr15:40695930-40695987 | Rare:11 | ||||
| chr15:40754619-40754809 | Common:1; Rare:54 |