| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34983328-34983386 | Common:1; Rare:11 | ||||
| chr14:35045992-35046327 | Common:1; Rare:99 | ||||
| chr14:35046332-35046760 | Common:5; Rare:153 | ||||
| chr14:35046828-35047006 | Common:2; Rare:40 | ||||
| chr14:35047102-35047375 | Common:2; Rare:47 | ||||
| chr14:35121188-35121569 | Common:2; Rare:88 | ||||
| chr14:35121634-35122179 | Common:3; Rare:150 | ||||
| chr14:35122208-35122343 | Rare:34 | ||||
| chr14:35122420-35122794 | Common:2; Rare:111 | ||||
| chr14:35122847-35123026 | Common:1; Rare:42 | ||||
| chr14:35291993-35292609 | Common:7; Rare:175; Clinvar:1 | ||||
| chr14:35292617-35292751 | Rare:36 | ||||
| chr14:35403146-35403347 | Rare:73; Clinvar:3 | ||||
| chr14:35403699-35404325 | Common:4; Rare:213; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:35404387-35404964 | Common:3; Rare:178; Clinvar:1; Clinvar (benign):5 |