| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103529022-103529243 | Common:1; Rare:67 | ||||
| chr14:103562282-103562375 | Rare:32 | ||||
| chr14:103562620-103563139 | Common:9; Rare:217; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103684268-103684345 | Rare:7 | ||||
| chr14:103715437-103715860 | Common:1; Rare:143 | ||||
| chr14:103742185-103742480 | Common:2; Rare:60 | ||||
| chr14:103742806-103742930 | Common:1; Rare:26 | ||||
| chr14:104048982-104049028 | Rare:4 | ||||
| chr14:104049143-104049457 | Common:2; Rare:46 | ||||
| chr14:104049617-104049903 | Common:3; Rare:47 | ||||
| chr14:104689483-104689681 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr14:104800409-104800670 | Common:2; Rare:72 | ||||
| chr14:104865160-104865424 | Common:2; Rare:71 | ||||
| chr14:104970469-104970567 | Common:2; Rare:20 | ||||
| chr14:104985662-104985823 | Common:2; Rare:63 |