| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:52729935-52730325 | Common:3; Rare:125 | ||||
| chr14:52730418-52730475 | Rare:31 | ||||
| chr14:52730489-52730532 | Rare:12 | ||||
| chr14:52730619-52730720 | Common:1; Rare:27 | ||||
| chr14:52791162-52791261 | Rare:18 | ||||
| chr14:52791397-52791955 | Common:3; Rare:161 | ||||
| chr14:52950360-52950386 | Rare:13 | ||||
| chr14:52950446-52950517 | Rare:24 | ||||
| chr14:52950767-52950868 | Common:1; Rare:33 | ||||
| chr14:52951006-52951241 | Common:1; Rare:70 | ||||
| chr14:52951293-52951499 | Common:2; Rare:70 | ||||
| chr14:53152427-53152546 | Rare:45; Clinvar (benign):1 | ||||
| chr14:53152788-53152909 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:53153007-53153493 | Common:4; Rare:166; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:53953392-53953710 | Common:2; Rare:86 |