| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102139678-102139936 | Rare:90 | ||||
| chr14:102305055-102305358 | Common:1; Rare:90 | ||||
| chr14:102362847-102363092 | Rare:112 | ||||
| chr14:102508373-102508706 | Common:3; Rare:58 | ||||
| chr14:103123331-103123471 | Rare:23 | ||||
| chr14:103333924-103334260 | Common:3; Rare:144 | ||||
| chr14:103521089-103521325 | Common:1; Rare:78 | ||||
| chr14:103529049-103529235 | Common:1; Rare:55 | ||||
| chr14:103562253-103562356 | Rare:43 | ||||
| chr14:103562624-103563063 | Common:8; Rare:175; Clinvar (benign):5 | ||||
| chr14:103715442-103715860 | Common:1; Rare:141 | ||||
| chr14:103942112-103942241 | Common:1; Rare:20 | ||||
| chr14:103942457-103942617 | Rare:37 | ||||
| chr14:104049335-104049423 | Rare:12 | ||||
| chr14:104723953-104724246 | Common:4; Rare:98 |