| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:18021640-18021785 | Rare:88 | ||||
| chr4:18021895-18021953 | Rare:15 | ||||
| chr4:20252739-20252890 | Common:1; Rare:32 | ||||
| chr4:20700337-20700548 | Common:3; Rare:92 | ||||
| chr4:21303968-21304118 | Common:16; Rare:50 | ||||
| chr4:22516052-22516185 | Common:2; Rare:44 | ||||
| chr4:23889892-23890245 | Common:1; Rare:63 | ||||
| chr4:23904080-23904387 | Rare:54 | ||||
| chr4:24584389-24584698 | Rare:101 | ||||
| chr4:25159875-25160177 | Common:3; Rare:80 | ||||
| chr4:25160358-25160727 | Common:3; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233835-25234108 | Rare:108 | ||||
| chr4:25376979-25377349 | Common:3; Rare:113 | ||||
| chr4:25655794-25655872 | Rare:20 | ||||
| chr4:25914051-25914364 | Common:3; Rare:132 |