| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333917-103334253 | Common:3; Rare:143 | ||||
| chr14:103521449-103521805 | Common:2; Rare:103 | ||||
| chr14:103529083-103529231 | Common:1; Rare:46 | ||||
| chr14:103562249-103562376 | Rare:48 | ||||
| chr14:103562623-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
| chr14:104724106-104724414 | Common:3; Rare:109; Clinvar:1 | ||||
| chr14:105419748-105420038 | Rare:92 | ||||
| chr14:105487044-105487216 | Common:1; Rare:45 | ||||
| chr15:25438982-25439249 | Common:2; Rare:105 | ||||
| chr15:29822020-29822215 | Rare:68 | ||||
| chr15:30903800-30903950 | Rare:38 | ||||
| chr15:31365915-31366163 | Common:2; Rare:62 | ||||
| chr15:32615117-32615159 | Common:1; Rare:13 | ||||
| chr15:34101820-34102117 | Common:1; Rare:65 | ||||
| chr15:34792088-34792575 | Rare:77; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):1 |