| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:71321062-71321158 | Common:1; Rare:32 | ||||
| chr14:73058330-73058579 | Common:3; Rare:75 | ||||
| chr14:73569020-73569088 | Rare:11 | ||||
| chr14:73569151-73569292 | Rare:43 | ||||
| chr14:73644900-73645030 | Common:2; Rare:37; Clinvar:2 | ||||
| chr14:73787121-73787355 | Common:2; Rare:83 | ||||
| chr14:73851733-73851974 | Common:4; Rare:82 | ||||
| chr14:73950078-73950323 | Common:5; Rare:96; Clinvar (benign):3 | ||||
| chr14:74019259-74019423 | Common:1; Rare:64 | ||||
| chr14:74493246-74493781 | Common:4; Rare:170; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713070-74713207 | Rare:71 | ||||
| chr14:75002584-75003026 | Common:1; Rare:141; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75064008-75064318 | Common:1; Rare:71 | ||||
| chr14:75127001-75127120 | Rare:38 | ||||
| chr14:75660819-75661334 | Common:4; Rare:122 |