| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75176085-75176259 | Common:1; Rare:34 | ||||
| chr14:75176278-75176421 | Rare:35 | ||||
| chr14:75176555-75176681 | Rare:51 | ||||
| chr14:75176852-75177053 | Rare:45 | ||||
| chr14:75278211-75278297 | Rare:16 | ||||
| chr14:75278332-75278924 | Common:5; Rare:140 | ||||
| chr14:75279343-75279568 | Common:1; Rare:46 | ||||
| chr14:75427222-75427477 | Rare:46 | ||||
| chr14:75427874-75428147 | Rare:62 | ||||
| chr14:75578460-75578726 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr14:75578835-75578972 | Common:3; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:75660786-75660999 | Rare:55 | ||||
| chr14:75661028-75661386 | Common:5; Rare:89 | ||||
| chr14:75661406-75661552 | Common:1; Rare:39 | ||||
| chr14:75981546-75981669 | Rare:20; Clinvar:2 |