| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562623-103563019 | Common:6; Rare:143; Clinvar (benign):2 | ||||
| chr14:103692234-103692330 | Rare:18 | ||||
| chr14:103715489-103715823 | Common:1; Rare:100 | ||||
| chr14:103921480-103921647 | Common:3; Rare:60 | ||||
| chr14:105021035-105021359 | Common:1; Rare:115 | ||||
| chr14:105398220-105398560 | Common:5; Rare:108 | ||||
| chr14:105419731-105420032 | Rare:97 | ||||
| chr15:22838481-22838704 | Common:2; Rare:92 | ||||
| chr15:23039545-23039753 | Common:1; Rare:82 | ||||
| chr15:25439001-25439227 | Common:2; Rare:84 | ||||
| chr15:29269792-29270055 | Common:1; Rare:87 | ||||
| chr15:30903620-30903943 | Common:3; Rare:83 | ||||
| chr15:32615086-32615603 | Common:7; Rare:130 | ||||
| chr15:34101843-34102117 | Common:1; Rare:54 | ||||
| chr15:34224933-34225105 | Rare:63 |