| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89243796-89243976 | Common:2; Rare:56; Clinvar:1 | ||||
| chr15:89679302-89679519 | Common:1; Rare:38 | ||||
| chr15:89893954-89894061 | Rare:36 | ||||
| chr15:89912839-89912913 | Rare:27 | ||||
| chr15:90233898-90234268 | Common:6; Rare:103 | ||||
| chr15:90265646-90265764 | Rare:62 | ||||
| chr15:90994476-90994832 | Common:1; Rare:128 | ||||
| chr15:93073108-93073324 | Common:3; Rare:81 | ||||
| chr15:99251221-99251524 | Common:4; Rare:115 | ||||
| chr15:100602140-100602630 | Common:3; Rare:133 | ||||
| chr15:101295174-101295386 | Rare:70 | ||||
| chr15:101652284-101652454 | Common:3; Rare:87 | ||||
| chr16:53590-53908 | Common:7; Rare:109 | ||||
| chr16:78175-78282 | Common:3; Rare:38 | ||||
| chr16:177065-177426 | Common:1; Rare:117; Clinvar:18; Clinvar (benign):3; Clinvar (pathogenic):3 |