| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45134346-45134769 | Rare:151 | ||||
| chr14:45134900-45135129 | Rare:48 | ||||
| chr14:45135701-45136045 | Common:1; Rare:84; Clinvar:1 | ||||
| chr14:45136174-45136241 | Rare:22; Clinvar:2 | ||||
| chr14:45252999-45253381 | Rare:108 | ||||
| chr14:45253387-45253651 | Common:2; Rare:101 | ||||
| chr14:45253698-45253942 | Common:1; Rare:61 | ||||
| chr14:45253993-45254312 | Rare:77 | ||||
| chr14:49585857-49586159 | Common:1; Rare:98; Clinvar (pathogenic):1 | ||||
| chr14:49586338-49586766 | Common:1; Rare:229 | ||||
| chr14:49598230-49598374 | Common:1; Rare:32 | ||||
| chr14:49598439-49599058 | Common:4; Rare:225 | ||||
| chr14:49599089-49599349 | Rare:79 | ||||
| chr14:49599353-49599721 | Common:2; Rare:71 | ||||
| chr14:49599724-49599991 | Common:4; Rare:69 |