| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56435446-56435992 | Common:6; Rare:180 | ||||
| chr4:56448500-56448821 | Common:2; Rare:61 | ||||
| chr4:56467524-56467734 | Common:2; Rare:84; Clinvar (benign):5 | ||||
| chr4:56907766-56907998 | Common:3; Rare:85 | ||||
| chr4:56977450-56977770 | Common:2; Rare:116 | ||||
| chr4:57110035-57110198 | Rare:59 | ||||
| chr4:65670429-65670617 | Rare:46 | ||||
| chr4:67701057-67701431 | Common:4; Rare:170 | ||||
| chr4:70688924-70689261 | Common:1; Rare:118 | ||||
| chr4:70839776-70840278 | Common:1; Rare:140 | ||||
| chr4:70902220-70902402 | Common:4; Rare:62 | ||||
| chr4:70993467-70993830 | Common:6; Rare:118 | ||||
| chr4:71186997-71187306 | Common:2; Rare:81 | ||||
| chr4:73104197-73104393 | Common:1; Rare:38 | ||||
| chr4:73258543-73258894 | Common:1; Rare:100 |