| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75008315-75009067 | Common:6; Rare:172; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75183017-75183640 | Common:5; Rare:125 | ||||
| chr14:75200480-75200990 | Common:2; Rare:127 | ||||
| chr14:75254260-75254880 | Common:2; Rare:127 | ||||
| chr14:75254890-75255430 | Common:6; Rare:237 | ||||
| chr14:75258640-75258880 | Common:2; Rare:61 | ||||
| chr14:75258871-75259441 | Common:6; Rare:357 | ||||
| chr14:75259991-75260570 | Common:2; Rare:154 | ||||
| chr14:75263861-75264410 | Common:9; Rare:248 | ||||
| chr14:75269215-75269619 | Rare:257 | ||||
| chr14:75273290-75273740 | Common:2; Rare:69 | ||||
| chr14:75276935-75277093 | Rare:29 | ||||
| chr14:75277004-75277368 | Common:2; Rare:130 | ||||
| chr14:75277434-75277756 | Common:2; Rare:109 | ||||
| chr14:75289830-75290280 | Common:4; Rare:74 |