| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53891816-53892021 | Common:2; Rare:63 | ||||
| chr3:56557081-56557245 | Common:2; Rare:64 | ||||
| chr3:56683020-56683371 | Common:4; Rare:120 | ||||
| chr3:56916385-56916527 | Rare:24 | ||||
| chr3:57079257-57079420 | Common:2; Rare:52 | ||||
| chr3:57227600-57227889 | Common:3; Rare:98 | ||||
| chr3:57555996-57556321 | Rare:81 | ||||
| chr3:57597331-57597811 | Common:7; Rare:143 | ||||
| chr3:58008334-58008433 | Common:1; Rare:38 | ||||
| chr3:58306450-58306552 | Common:1; Rare:40 | ||||
| chr3:58332800-58332973 | Common:3; Rare:49 | ||||
| chr3:58433814-58433935 | Rare:44; Clinvar (benign):1 | ||||
| chr3:60081224-60081331 | Common:1; Rare:26 | ||||
| chr3:62875327-62875402 | Common:1; Rare:20 | ||||
| chr3:63863777-63864110 | Common:7; Rare:111 |