| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14947975-14948917 | Common:18; Rare:1415 | ||||
| chr3:15065151-15065551 | Common:17; Rare:382 | ||||
| chr3:15098634-15099408 | Common:5; Rare:473 | ||||
| chr3:15205803-15206314 | Common:3; Rare:752 | ||||
| chr3:15331493-15332361 | Common:7; Rare:268 | ||||
| chr3:15332320-15333887 | Common:23; Rare:616 | ||||
| chr3:15427375-15428047 | Common:9; Rare:551 | ||||
| chr3:15601419-15602221 | Common:37; Rare:1341; Clinvar:22; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr3:15630008-15630929 | Common:2; Rare:361 | ||||
| chr3:15796335-15798451 | Common:45; Rare:992 | ||||
| chr3:15858802-15859049 | Common:2; Rare:82 | ||||
| chr3:15859490-15859710 | Common:8; Rare:100 | ||||
| chr3:15859692-15860240 | Common:26; Rare:740 | ||||
| chr3:16264090-16264821 | Common:8; Rare:406 | ||||
| chr3:16264831-16265300 | Common:19; Rare:918 |