| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52659194-52659442 | Common:1; Rare:83 | ||||
| chr4:52862159-52862322 | Common:6; Rare:74 | ||||
| chr4:55395866-55395957 | Rare:24; Clinvar:2 | ||||
| chr4:56387428-56387524 | Rare:34 | ||||
| chr4:56435560-56435765 | Common:3; Rare:68 | ||||
| chr4:56467532-56467689 | Common:2; Rare:68; Clinvar (benign):4 | ||||
| chr4:56977581-56977763 | Common:1; Rare:67 | ||||
| chr4:57110357-57110560 | Common:2; Rare:62 | ||||
| chr4:67701111-67701358 | Common:4; Rare:118 | ||||
| chr4:70688474-70688567 | Common:2; Rare:23 | ||||
| chr4:70902181-70902402 | Common:5; Rare:77 | ||||
| chr4:70993528-70993664 | Common:4; Rare:41 | ||||
| chr4:71187179-71187324 | Common:1; Rare:45 | ||||
| chr4:73258530-73258887 | Common:1; Rare:98 | ||||
| chr4:75514273-75514505 | Common:1; Rare:80 |