| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67619671-67619965 | Common:2; Rare:116 | ||||
| chr14:67674567-67675180 | Common:4; Rare:214 | ||||
| chr14:67695668-67695887 | Common:2; Rare:137 | ||||
| chr14:67816551-67816765 | Rare:68; Clinvar:1 | ||||
| chr14:67819634-67819847 | Rare:93 | ||||
| chr14:68000093-68000265 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr14:68792973-68793360 | Common:2; Rare:179 | ||||
| chr14:68795231-68795505 | Common:5; Rare:66 | ||||
| chr14:68795701-68795896 | Common:4; Rare:119 | ||||
| chr14:68796000-68796237 | Rare:130 | ||||
| chr14:68796280-68796690 | Common:5; Rare:115 | ||||
| chr14:68977680-68978060 | Common:12; Rare:161 | ||||
| chr14:68978149-68978549 | Common:2; Rare:101 | ||||
| chr14:68978692-68978841 | Common:2; Rare:68 | ||||
| chr14:68979138-68979595 | Common:5; Rare:257 |