| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:54509569-54509965 | Common:6; Rare:134 | ||||
| chr14:54566493-54566727 | Rare:70 | ||||
| chr14:54566888-54567049 | Rare:38 | ||||
| chr14:54567491-54567746 | Common:2; Rare:52 | ||||
| chr14:54567929-54568060 | Rare:31 | ||||
| chr14:54652197-54652521 | Rare:52 | ||||
| chr14:54652905-54652977 | Rare:13 | ||||
| chr14:54902211-54902326 | Common:1; Rare:41; Clinvar (pathogenic):1 | ||||
| chr14:54902747-54902979 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:55026744-55026879 | Rare:33 | ||||
| chr14:55026927-55027337 | Common:2; Rare:107 | ||||
| chr14:55027392-55027599 | Rare:33 | ||||
| chr14:55051305-55052213 | Common:3; Rare:317 | ||||
| chr14:55129575-55129754 | Rare:40 | ||||
| chr14:55191110-55191171 | Rare:3 |