| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:60091640-60092420 | Common:38; Rare:1068 | ||||
| chr14:60092450-60092953 | Common:8; Rare:226 | ||||
| chr14:60164399-60164799 | Common:1; Rare:73 | ||||
| chr14:60164702-60164895 | Common:1; Rare:58 | ||||
| chr14:60165148-60165759 | Common:4; Rare:349 | ||||
| chr14:60248880-60249390 | Common:25; Rare:954 | ||||
| chr14:60249292-60249692 | Common:3; Rare:201 | ||||
| chr14:60249650-60250120 | Common:8; Rare:390 | ||||
| chr14:60250353-60250753 | Common:1; Rare:101 | ||||
| chr14:60485132-60485532 | Common:1; Rare:95 | ||||
| chr14:60485670-60486338 | Common:20; Rare:521 | ||||
| chr14:60649170-60649710 | Common:11; Rare:305; Clinvar:6; Clinvar (benign):5 | ||||
| chr14:60722651-60723408 | Common:5; Rare:650 | ||||
| chr14:60723340-60724015 | Rare:541 | ||||
| chr14:60724240-60724590 | Common:5; Rare:297 |