| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91509258-91509500 | Common:1; Rare:73 | ||||
| chr14:91509737-91509801 | Rare:23 | ||||
| chr14:91509856-91510133 | Common:1; Rare:86 | ||||
| chr14:91510151-91510425 | Rare:99 | ||||
| chr14:91510434-91510712 | Common:1; Rare:97 | ||||
| chr14:91510787-91510926 | Rare:34 | ||||
| chr14:91511034-91511097 | Common:1; Rare:12 | ||||
| chr14:91947309-91947477 | Common:3; Rare:33; Clinvar (benign):2 | ||||
| chr14:91947562-91947668 | Common:1; Rare:30; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92039691-92039850 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:92039942-92040262 | Common:4; Rare:91; Clinvar:5; Clinvar (benign):2 | ||||
| chr14:92040330-92040484 | Common:1; Rare:24 | ||||
| chr14:92106055-92106232 | Rare:41 | ||||
| chr14:92106276-92106383 | Rare:35 | ||||
| chr14:92106495-92106868 | Common:3; Rare:112 |