| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:52730408-52730719 | Common:2; Rare:102 | ||||
| chr14:52790992-52791071 | Rare:11 | ||||
| chr14:52791094-52791351 | Common:1; Rare:46 | ||||
| chr14:52791380-52791965 | Common:3; Rare:166 | ||||
| chr14:52792072-52792297 | Common:1; Rare:27 | ||||
| chr14:52873803-52874009 | Common:3; Rare:46 | ||||
| chr14:52950338-52950510 | Common:1; Rare:62 | ||||
| chr14:52950739-52951255 | Common:2; Rare:156 | ||||
| chr14:52951271-52951534 | Common:5; Rare:94 | ||||
| chr14:53151906-53152175 | Common:4; Rare:45 | ||||
| chr14:53152325-53152736 | Common:2; Rare:165; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:53152773-53152915 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:53152940-53153109 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:53153112-53153511 | Common:4; Rare:140 | ||||
| chr14:53953378-53953745 | Common:2; Rare:100 |