| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:53377431-53377718 | Common:3; Rare:86 | ||||
| chr4:55948736-55948847 | Rare:20 | ||||
| chr4:56387198-56387556 | Rare:100 | ||||
| chr4:56435484-56435767 | Common:5; Rare:102 | ||||
| chr4:56435977-56436307 | Rare:114 | ||||
| chr4:56467524-56467734 | Common:2; Rare:84; Clinvar (benign):5 | ||||
| chr4:56977597-56977727 | Common:1; Rare:47 | ||||
| chr4:67701118-67701411 | Common:4; Rare:136 | ||||
| chr4:68349985-68350227 | Common:2; Rare:86 | ||||
| chr4:70688421-70688543 | Common:1; Rare:33 | ||||
| chr4:70688908-70688942 | Rare:11 | ||||
| chr4:70993416-70993715 | Common:5; Rare:97 | ||||
| chr4:73069674-73069994 | Common:2; Rare:135 | ||||
| chr4:73223041-73223160 | Rare:22 | ||||
| chr4:73258793-73258906 | Rare:34 |