| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56467385-56467703 | Common:13; Rare:654; Clinvar (benign):25 | ||||
| chr4:56467707-56468412 | Common:4; Rare:250 | ||||
| chr4:56530268-56531004 | Common:28; Rare:477 | ||||
| chr4:56530974-56531374 | Common:4; Rare:139 | ||||
| chr4:56907615-56908056 | Common:15; Rare:396 | ||||
| chr4:56908108-56908535 | Common:3; Rare:158 | ||||
| chr4:56908451-56909191 | Common:25; Rare:717 | ||||
| chr4:56977420-56977900 | Common:14; Rare:717 | ||||
| chr4:56977997-56978586 | Common:8; Rare:145 | ||||
| chr4:56978660-56978992 | Common:18; Rare:292 | ||||
| chr4:56979058-56979462 | Common:2; Rare:163 | ||||
| chr4:57110219-57111329 | Common:11; Rare:374 | ||||
| chr4:65670370-65670860 | Common:3; Rare:117 | ||||
| chr4:67514182-67515001 | Common:4; Rare:329 | ||||
| chr4:67545287-67545398 | Common:1; Rare:32 |