| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23301176-23301428 | Common:3; Rare:53 | ||||
| chr14:23301470-23301684 | Rare:79 | ||||
| chr14:23301696-23302044 | Common:1; Rare:108 | ||||
| chr14:23306162-23306562 | Common:3; Rare:83 | ||||
| chr14:23306605-23306891 | Common:1; Rare:63 | ||||
| chr14:23321149-23321506 | Common:2; Rare:108; Clinvar (pathogenic):1 | ||||
| chr14:23321864-23321998 | Common:1; Rare:35 | ||||
| chr14:23352793-23352948 | Rare:40 | ||||
| chr14:23366251-23366523 | Rare:66 | ||||
| chr14:23469501-23469761 | Common:1; Rare:74 | ||||
| chr14:23551060-23551490 | Common:2; Rare:68 | ||||
| chr14:23551510-23551930 | Common:1; Rare:106 | ||||
| chr14:23555909-23556082 | Common:1; Rare:46 | ||||
| chr14:23556184-23556371 | Common:2; Rare:37 | ||||
| chr14:23567630-23567980 | Common:1; Rare:72 |