| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23286040-23286447 | Common:2; Rare:109 | ||||
| chr14:23286534-23286662 | Rare:25 | ||||
| chr14:23301131-23301645 | Common:3; Rare:140 | ||||
| chr14:23301689-23302052 | Common:1; Rare:113 | ||||
| chr14:23302304-23302540 | Common:1; Rare:74 | ||||
| chr14:23302763-23302908 | Rare:30 | ||||
| chr14:23306634-23306980 | Common:1; Rare:73 | ||||
| chr14:23307255-23307383 | Rare:24 | ||||
| chr14:23320836-23321550 | Common:5; Rare:194; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr14:23321680-23321844 | Common:1; Rare:48 | ||||
| chr14:23322134-23322207 | Rare:30 | ||||
| chr14:23322264-23322347 | Rare:23 | ||||
| chr14:23322549-23322670 | Rare:19 | ||||
| chr14:23352375-23352395 | Rare:3 | ||||
| chr14:23352776-23352942 | Rare:44 |