| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44427269-44427653 | Common:1; Rare:96 | ||||
| chr15:44536529-44536586 | Rare:14 | ||||
| chr15:44536663-44537401 | Common:3; Rare:242 | ||||
| chr15:44663531-44663888 | Rare:161; Clinvar:13; Clinvar (benign):6 | ||||
| chr15:44711341-44711611 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728869-44729198 | Common:1; Rare:70 | ||||
| chr15:45023051-45023237 | Common:3; Rare:50 | ||||
| chr15:45200492-45200658 | Common:1; Rare:47 | ||||
| chr15:45201095-45201153 | Common:1; Rare:28 | ||||
| chr15:45378475-45378634 | Common:3; Rare:45; Clinvar:1; Clinvar (benign):3 | ||||
| chr15:45402168-45402336 | Common:1; Rare:52 | ||||
| chr15:45587096-45587470 | Common:1; Rare:90; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:45587696-45587818 | Common:2; Rare:28 | ||||
| chr15:47717170-47717579 | Common:2; Rare:86 | ||||
| chr15:47717863-47718113 | Common:2; Rare:54 |