| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53130398-53130556 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347518-53347734 | Common:1; Rare:68 | ||||
| chr3:53846417-53846573 | Rare:50 | ||||
| chr3:53891794-53892035 | Common:2; Rare:72 | ||||
| chr3:56557076-56557238 | Common:2; Rare:63 | ||||
| chr3:56683015-56683358 | Common:4; Rare:119 | ||||
| chr3:56801905-56802053 | Rare:55 | ||||
| chr3:56916383-56916531 | Rare:24 | ||||
| chr3:57079251-57079369 | Common:1; Rare:42 | ||||
| chr3:57227591-57227922 | Common:4; Rare:113 | ||||
| chr3:57556032-57556315 | Rare:68 | ||||
| chr3:57597330-57597792 | Common:6; Rare:136 | ||||
| chr3:57756045-57756313 | Rare:69 | ||||
| chr3:57889883-57890079 | Rare:41; Clinvar (benign):2 | ||||
| chr3:58008344-58008456 | Common:1; Rare:46; Clinvar:1 |