| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50944406-50944580 | Common:4; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51240009-51240287 | Common:2; Rare:93 | ||||
| chr14:51651636-51651984 | Common:4; Rare:100 | ||||
| chr14:52069000-52069232 | Common:2; Rare:51 | ||||
| chr14:52695518-52695858 | Common:1; Rare:97 | ||||
| chr14:52707040-52707232 | Common:1; Rare:84 | ||||
| chr14:52791623-52791955 | Common:3; Rare:102 | ||||
| chr14:55027048-55027290 | Common:2; Rare:69 | ||||
| chr14:55051345-55051722 | Common:1; Rare:144 | ||||
| chr14:55191538-55191705 | Common:4; Rare:38 | ||||
| chr14:55580127-55580285 | Common:1; Rare:70 | ||||
| chr14:57268821-57269094 | Common:2; Rare:85 | ||||
| chr14:58199823-58200199 | Common:4; Rare:148 | ||||
| chr14:58298108-58298386 | Rare:72 | ||||
| chr14:58427529-58427741 | Rare:71 |