| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105021044-105021371 | Common:1; Rare:115 | ||||
| chr14:105300996-105301121 | Rare:26 | ||||
| chr14:105419733-105420032 | Rare:95 | ||||
| chr14:105487542-105487812 | Common:2; Rare:80 | ||||
| chr15:22838356-22838710 | Common:3; Rare:127 | ||||
| chr15:22980690-22981016 | Common:4; Rare:105 | ||||
| chr15:23565602-23565685 | Rare:28 | ||||
| chr15:23687234-23687414 | Common:1; Rare:66 | ||||
| chr15:24954879-24955100 | Rare:102 | ||||
| chr15:25438979-25439229 | Common:3; Rare:95 | ||||
| chr15:26773705-26774019 | Common:3; Rare:87; Clinvar (benign):1 | ||||
| chr15:28099616-28099810 | Common:1; Rare:31 | ||||
| chr15:29269779-29269929 | Common:1; Rare:62 | ||||
| chr15:29822206-29822602 | Common:2; Rare:151 | ||||
| chr15:30903705-30903742 | Rare:3 |