| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74782389-74782495 | Rare:38 | ||||
| chr15:74782990-74783058 | Rare:11 | ||||
| chr15:74842651-74842945 | Rare:61 | ||||
| chr15:74843052-74843457 | Common:2; Rare:118 | ||||
| chr15:74872942-74873224 | Common:2; Rare:79 | ||||
| chr15:74873268-74873500 | Common:6; Rare:69 | ||||
| chr15:74889939-74890155 | Rare:90; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74890567-74890626 | Common:1; Rare:23 | ||||
| chr15:74890635-74890658 | Rare:6; Clinvar:1 | ||||
| chr15:74905477-74905995 | Rare:86 | ||||
| chr15:74906044-74906201 | Rare:26 | ||||
| chr15:74906218-74906360 | Rare:59 | ||||
| chr15:74906491-74906990 | Common:2; Rare:178 | ||||
| chr15:74907287-74907313 | Rare:4 | ||||
| chr15:74937532-74937615 | Rare:17 |