| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:54123166-54123524 | Common:4; Rare:87 | ||||
| chr3:56557081-56557230 | Common:2; Rare:57 | ||||
| chr3:56682884-56683295 | Common:5; Rare:148 | ||||
| chr3:56801888-56802032 | Rare:52 | ||||
| chr3:57227600-57227919 | Common:3; Rare:107 | ||||
| chr3:57555996-57556321 | Rare:81 | ||||
| chr3:57597287-57597668 | Common:4; Rare:119 | ||||
| chr3:58008282-58008423 | Common:2; Rare:53 | ||||
| chr3:58306109-58306318 | Common:1; Rare:58 | ||||
| chr3:58433787-58433944 | Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:62242841-62243117 | Rare:54 | ||||
| chr3:62318890-62319076 | Rare:77 | ||||
| chr3:62373478-62373543 | Rare:11 | ||||
| chr3:63863743-63864128 | Common:7; Rare:129 | ||||
| chr3:64268166-64268336 | Rare:36 |