| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:30622190-30622350 | Rare:57 | ||||
| chr14:31025572-31025664 | Common:1; Rare:21 | ||||
| chr14:31121443-31121686 | Common:2; Rare:60 | ||||
| chr14:31207466-31207847 | Common:2; Rare:125 | ||||
| chr14:31208158-31208264 | Common:1; Rare:28 | ||||
| chr14:31420526-31420763 | Common:3; Rare:71 | ||||
| chr14:31457350-31457577 | Common:2; Rare:80 | ||||
| chr14:31561322-31561491 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076141-32076326 | Rare:56 | ||||
| chr14:32076676-32077053 | Common:3; Rare:110 | ||||
| chr14:34462214-34462582 | Common:1; Rare:128 | ||||
| chr14:34630112-34630256 | Common:5; Rare:70 | ||||
| chr14:34714553-34714770 | Common:3; Rare:78 | ||||
| chr14:34875271-34875530 | Common:1; Rare:94 | ||||
| chr14:34982372-34982682 | Common:1; Rare:121 |