| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44711360-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023041-45023267 | Common:3; Rare:57 | ||||
| chr15:45378466-45378692 | Common:4; Rare:61; Clinvar:1; Clinvar (benign):4 | ||||
| chr15:45522557-45522677 | Rare:30 | ||||
| chr15:45587110-45587660 | Common:1; Rare:160; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:47183908-47184379 | Common:3; Rare:146 | ||||
| chr15:47184573-47184795 | Common:2; Rare:53 | ||||
| chr15:47717197-47717549 | Common:1; Rare:75 | ||||
| chr15:48331367-48331440 | Rare:22 | ||||
| chr15:48645710-48645913 | Common:2; Rare:65; Clinvar (benign):1 | ||||
| chr15:48877993-48878395 | Rare:150 | ||||
| chr15:48963114-48963244 | Common:1; Rare:21 | ||||
| chr15:49155523-49155845 | Common:2; Rare:108 | ||||
| chr15:49170128-49170298 | Rare:38 | ||||
| chr15:49620799-49621107 | Common:6; Rare:122 |