| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102083544-102083985 | Common:3; Rare:179 | ||||
| chr14:102086968-102087314 | Common:4; Rare:138 | ||||
| chr14:102139291-102139441 | Rare:66 | ||||
| chr14:102139641-102139939 | Rare:106 | ||||
| chr14:102305033-102305288 | Common:1; Rare:77 | ||||
| chr14:102316878-102317113 | Common:4; Rare:99 | ||||
| chr14:102362847-102363092 | Rare:112 | ||||
| chr14:103123290-103123477 | Rare:33 | ||||
| chr14:103333897-103334258 | Common:3; Rare:151 | ||||
| chr14:103385233-103385439 | Common:1; Rare:79 | ||||
| chr14:103520473-103520840 | Common:2; Rare:99 | ||||
| chr14:103521092-103521531 | Common:2; Rare:139; Clinvar:1 | ||||
| chr14:103522824-103522941 | Rare:38 | ||||
| chr14:103528981-103529260 | Common:1; Rare:79 | ||||
| chr14:103562620-103563085 | Common:8; Rare:183; Clinvar (benign):5 |