| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333931-103334252 | Common:3; Rare:133 | ||||
| chr14:103521092-103521194 | Common:1; Rare:30 | ||||
| chr14:103529142-103529233 | Common:1; Rare:35 | ||||
| chr14:103562624-103563085 | Common:8; Rare:182; Clinvar (benign):5 | ||||
| chr14:103715489-103715853 | Common:1; Rare:117 | ||||
| chr14:104752998-104753208 | Common:2; Rare:79 | ||||
| chr14:104970476-104970567 | Common:2; Rare:17 | ||||
| chr14:105419733-105420038 | Rare:97 | ||||
| chr15:25439035-25439261 | Common:1; Rare:91 | ||||
| chr15:30903698-30903952 | Common:1; Rare:63 | ||||
| chr15:32615163-32615571 | Common:5; Rare:102 | ||||
| chr15:33310661-33311013 | Common:1; Rare:103 | ||||
| chr15:34101843-34102083 | Common:1; Rare:48 | ||||
| chr15:34795504-34795669 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:34988236-34988365 | Rare:55 |