| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:52950849-52950965 | Rare:36 | ||||
| chr14:52951014-52951118 | Rare:21 | ||||
| chr14:52951143-52951508 | Common:3; Rare:145 | ||||
| chr14:52951813-52952099 | Common:2; Rare:60 | ||||
| chr14:53152374-53152725 | Common:2; Rare:142; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:53152774-53152796 | Common:1; Rare:19; Clinvar (benign):1 | ||||
| chr14:53152962-53153083 | Rare:38; Clinvar:1 | ||||
| chr14:53153148-53153515 | Common:4; Rare:131 | ||||
| chr14:53953391-53953616 | Common:2; Rare:64 | ||||
| chr14:54396662-54397114 | Common:2; Rare:121 | ||||
| chr14:54440859-54441052 | Common:2; Rare:59 | ||||
| chr14:54441054-54441158 | Common:1; Rare:40 | ||||
| chr14:54441195-54441541 | Rare:120 | ||||
| chr14:54488839-54489248 | Common:4; Rare:108 | ||||
| chr14:54509242-54509510 | Rare:59 |