| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:55580088-55580331 | Common:2; Rare:105 | ||||
| chr14:57268526-57268614 | Rare:23 | ||||
| chr14:57268635-57269094 | Common:2; Rare:146 | ||||
| chr14:57283007-57283180 | Rare:45 | ||||
| chr14:57390401-57390639 | Common:1; Rare:65 | ||||
| chr14:58247466-58247758 | Rare:52 | ||||
| chr14:58270241-58270442 | Common:1; Rare:56 | ||||
| chr14:58298077-58298662 | Rare:163 | ||||
| chr14:58427028-58427384 | Common:3; Rare:77 | ||||
| chr14:58427509-58427765 | Rare:86 | ||||
| chr14:59483719-59484137 | Common:5; Rare:151 | ||||
| chr14:59484289-59484594 | Common:3; Rare:129 | ||||
| chr14:60091728-60092051 | Common:5; Rare:121 | ||||
| chr14:60092107-60092516 | Common:7; Rare:130 | ||||
| chr14:60649427-60649657 | Common:3; Rare:68; Clinvar (benign):1 |