| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57078782-57078920 | Rare:35 | ||||
| chr3:57227568-57227925 | Common:4; Rare:122 | ||||
| chr3:57555996-57556336 | Rare:85 | ||||
| chr3:57597076-57597751 | Common:5; Rare:203 | ||||
| chr3:57692957-57693160 | Common:1; Rare:60 | ||||
| chr3:57756135-57756309 | Rare:42 | ||||
| chr3:58237423-58237600 | Common:7; Rare:55 | ||||
| chr3:58306137-58306328 | Common:1; Rare:57 | ||||
| chr3:58433770-58434082 | Common:2; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58491743-58491909 | Common:1; Rare:44 | ||||
| chr3:61251364-61251597 | Common:4; Rare:55 | ||||
| chr3:61561447-61561662 | Common:2; Rare:70 | ||||
| chr3:62243635-62243846 | Common:1; Rare:43 | ||||
| chr3:62318881-62319062 | Rare:75 | ||||
| chr3:62875343-62875397 | Common:1; Rare:12 |