| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74881736-74881959 | Common:1; Rare:92 | ||||
| chr14:74955591-74955752 | Common:1; Rare:36 | ||||
| chr14:75002734-75002975 | Common:1; Rare:74; Clinvar:2 | ||||
| chr14:75051418-75051535 | Common:2; Rare:36; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75069443-75069722 | Common:2; Rare:74 | ||||
| chr14:75126882-75127120 | Rare:79 | ||||
| chr14:75427671-75427731 | Rare:14 | ||||
| chr14:75578523-75578650 | Common:2; Rare:25; Clinvar (benign):1 | ||||
| chr14:75660789-75661346 | Common:4; Rare:136 | ||||
| chr14:75661498-75661619 | Rare:24 | ||||
| chr14:76151746-76151982 | Rare:87 | ||||
| chr14:76310171-76310486 | Common:2; Rare:65 | ||||
| chr14:77098001-77098361 | Rare:113 | ||||
| chr14:77320834-77321105 | Rare:82; Clinvar:1 | ||||
| chr14:77377052-77377433 | Common:2; Rare:119 |