| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75126882-75127110 | Rare:74 | ||||
| chr14:75147707-75147897 | Common:3; Rare:36 | ||||
| chr14:75278356-75278689 | Common:1; Rare:81 | ||||
| chr14:75279430-75279870 | Common:1; Rare:86 | ||||
| chr14:75280363-75280954 | Common:4; Rare:141 | ||||
| chr14:75427653-75427731 | Rare:19 | ||||
| chr14:75660800-75661320 | Common:4; Rare:125 | ||||
| chr14:75661517-75661619 | Rare:17 | ||||
| chr14:77097980-77098354 | Rare:122 | ||||
| chr14:77320785-77321094 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:77376976-77377415 | Common:5; Rare:128 | ||||
| chr14:77457556-77457876 | Common:1; Rare:94 | ||||
| chr14:77707985-77708122 | Rare:67 | ||||
| chr14:77800005-77800145 | Rare:24 | ||||
| chr14:81220723-81221069 | Common:3; Rare:140 |