| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:55580080-55580351 | Common:2; Rare:114 | ||||
| chr14:55672632-55672989 | Common:2; Rare:94 | ||||
| chr14:57268638-57269094 | Common:2; Rare:145 | ||||
| chr14:58244630-58244939 | Rare:103 | ||||
| chr14:58298077-58298604 | Rare:141 | ||||
| chr14:58427051-58427411 | Common:3; Rare:82 | ||||
| chr14:58427498-58427812 | Rare:93 | ||||
| chr14:59188480-59188735 | Common:1; Rare:61 | ||||
| chr14:59483682-59484047 | Common:5; Rare:120 | ||||
| chr14:59484289-59484593 | Common:3; Rare:129 | ||||
| chr14:60091794-60092057 | Common:5; Rare:92 | ||||
| chr14:60249500-60249651 | Rare:43 | ||||
| chr14:60649442-60649711 | Common:3; Rare:77; Clinvar (benign):1 | ||||
| chr14:60649831-60650231 | Common:3; Rare:78 | ||||
| chr14:60653092-60653197 | Rare:20 |