| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:51843400-51843713 | Rare:82 | ||||
| chr4:52659191-52659439 | Common:1; Rare:83 | ||||
| chr4:53365972-53366129 | Rare:30 | ||||
| chr4:55546806-55547080 | Common:2; Rare:100 | ||||
| chr4:56387414-56387524 | Rare:36 | ||||
| chr4:56435458-56435772 | Common:5; Rare:113 | ||||
| chr4:56467542-56467723 | Common:2; Rare:74; Clinvar (benign):5 | ||||
| chr4:56977574-56977785 | Common:1; Rare:81 | ||||
| chr4:57109877-57110063 | Rare:61 | ||||
| chr4:67545434-67545742 | Common:2; Rare:77 | ||||
| chr4:67701047-67701429 | Common:4; Rare:171 | ||||
| chr4:68349936-68350210 | Common:1; Rare:98 | ||||
| chr4:68951070-68951312 | Rare:102 | ||||
| chr4:69096380-69096519 | Common:2; Rare:29 | ||||
| chr4:69096716-69097235 | Common:2; Rare:167 |