| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53891802-53892088 | Common:5; Rare:97 | ||||
| chr3:56557086-56557226 | Common:2; Rare:53 | ||||
| chr3:57227591-57227911 | Common:3; Rare:111 | ||||
| chr3:57556006-57556331 | Rare:78 | ||||
| chr3:57597295-57597577 | Common:4; Rare:86 | ||||
| chr3:57692990-57693193 | Common:1; Rare:60 | ||||
| chr3:58008524-58008849 | Rare:80; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:58237275-58237576 | Common:7; Rare:78 | ||||
| chr3:58433782-58433992 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58537157-58537284 | Common:1; Rare:26 | ||||
| chr3:58537307-58537561 | Rare:35 | ||||
| chr3:58666700-58666985 | Common:1; Rare:48 | ||||
| chr3:61251312-61251607 | Common:4; Rare:70 | ||||
| chr3:61561412-61561649 | Common:2; Rare:83 | ||||
| chr3:63863777-63864158 | Common:8; Rare:127 |