| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43370923-43371209 | Common:4; Rare:76 | ||||
| chr15:43493092-43493340 | Common:1; Rare:75 | ||||
| chr15:43648710-43649025 | Common:3; Rare:134 | ||||
| chr15:43746261-43746705 | Common:3; Rare:175 | ||||
| chr15:43777114-43777405 | Rare:65 | ||||
| chr15:43824531-43824805 | Common:2; Rare:86 | ||||
| chr15:44288406-44288743 | Common:38; Rare:214 | ||||
| chr15:44536855-44537401 | Common:3; Rare:200 | ||||
| chr15:44711314-44711612 | Rare:89; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711731-44711989 | Rare:46 | ||||
| chr15:45201108-45201153 | Common:1; Rare:23 | ||||
| chr15:45378385-45378658 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):11 | ||||
| chr15:45402174-45402354 | Common:2; Rare:53 | ||||
| chr15:45587300-45587503 | Rare:64; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:45634590-45635107 | Common:2; Rare:136 |