| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105021047-105021387 | Common:1; Rare:119 | ||||
| chr14:105419711-105420032 | Common:1; Rare:100 | ||||
| chr15:22786506-22786752 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:23039541-23039664 | Common:1; Rare:56 | ||||
| chr15:23565428-23565685 | Common:1; Rare:69 | ||||
| chr15:23566218-23566359 | Rare:73; Clinvar (pathogenic):1 | ||||
| chr15:24954881-24955036 | Rare:77 | ||||
| chr15:25438984-25439261 | Common:2; Rare:112 | ||||
| chr15:28099277-28099502 | Common:2; Rare:78; Clinvar:1 | ||||
| chr15:28885801-28886184 | Common:2; Rare:117 | ||||
| chr15:30903779-30903943 | Rare:41 | ||||
| chr15:32615111-32615599 | Common:7; Rare:123 | ||||
| chr15:32641461-32641766 | Common:2; Rare:69 | ||||
| chr15:33194707-33194953 | Common:1; Rare:69 | ||||
| chr15:33310544-33310788 | Common:2; Rare:68 |