| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104970471-104970692 | Common:3; Rare:33 | ||||
| chr14:105419733-105420046 | Rare:98 | ||||
| chr15:23039539-23039693 | Common:1; Rare:63 | ||||
| chr15:23687235-23687415 | Common:1; Rare:66 | ||||
| chr15:25438984-25439227 | Common:2; Rare:91 | ||||
| chr15:29822020-29822182 | Rare:60 | ||||
| chr15:30903632-30903936 | Common:2; Rare:80 | ||||
| chr15:32615117-32615599 | Common:7; Rare:120 | ||||
| chr15:32641664-32641766 | Common:2; Rare:29 | ||||
| chr15:33310647-33311016 | Common:1; Rare:106 | ||||
| chr15:34101821-34102117 | Common:1; Rare:65 | ||||
| chr15:34224970-34225098 | Rare:46 | ||||
| chr15:34343071-34343443 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:34367186-34367290 | Rare:37 | ||||
| chr15:34582851-34582902 | Rare:18 |