| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75278871-75279170 | Common:1; Rare:87 | ||||
| chr14:75279431-75280131 | Common:3; Rare:163 | ||||
| chr14:75427903-75428050 | Rare:23 | ||||
| chr14:75660781-75661636 | Common:8; Rare:215 | ||||
| chr14:75985697-75985802 | Rare:47; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:77098019-77098364 | Rare:102 | ||||
| chr14:77320766-77321178 | Common:2; Rare:124; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:77321224-77321498 | Common:5; Rare:143 | ||||
| chr14:77377066-77377415 | Common:2; Rare:100 | ||||
| chr14:77457499-77458269 | Common:2; Rare:209 | ||||
| chr14:77468035-77468519 | Common:9; Rare:124 | ||||
| chr14:77616552-77616749 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):3 | ||||
| chr14:77707998-77708213 | Common:2; Rare:108 | ||||
| chr14:77799805-77800153 | Common:3; Rare:61 | ||||
| chr14:80941694-80941939 | Common:3; Rare:55 |