| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100376264-100376495 | Common:3; Rare:77 | ||||
| chr14:101809716-101809887 | Rare:36 | ||||
| chr14:102139667-102139914 | Rare:84 | ||||
| chr14:102362862-102363092 | Rare:103 | ||||
| chr14:103123206-103123477 | Rare:48 | ||||
| chr14:103562623-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
| chr14:103715466-103715851 | Common:1; Rare:126 | ||||
| chr14:105021031-105021386 | Common:1; Rare:127 | ||||
| chr15:22838356-22838717 | Common:3; Rare:129 | ||||
| chr15:23039546-23039753 | Common:1; Rare:81 | ||||
| chr15:24954879-24954999 | Rare:51 | ||||
| chr15:32615237-32615607 | Common:4; Rare:87 | ||||
| chr15:34101821-34102083 | Common:1; Rare:59 | ||||
| chr15:34224989-34225127 | Rare:55 | ||||
| chr15:34988209-34988382 | Common:1; Rare:73 |