| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104752836-104753257 | Common:3; Rare:148 | ||||
| chr14:104773549-104773640 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:104924818-104924884 | Rare:12 | ||||
| chr14:104970477-104970753 | Common:4; Rare:57 | ||||
| chr14:105300508-105300836 | Common:1; Rare:87 | ||||
| chr14:105419347-105419432 | Rare:14 | ||||
| chr14:105487032-105487284 | Common:2; Rare:84 | ||||
| chr15:22980297-22980490 | Rare:69 | ||||
| chr15:23687248-23687478 | Common:1; Rare:80 | ||||
| chr15:25438969-25439237 | Common:3; Rare:103 | ||||
| chr15:29822443-29822675 | Common:2; Rare:97 | ||||
| chr15:30903800-30903944 | Rare:36 | ||||
| chr15:31392378-31392511 | Rare:34 | ||||
| chr15:32615099-32615596 | Common:7; Rare:126 | ||||
| chr15:34101814-34102092 | Common:1; Rare:62 |