| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56450477-56450690 | Rare:43 | ||||
| chr4:56478379-56478609 | Common:2; Rare:53; Clinvar (benign):1 | ||||
| chr4:56994962-56995343 | Common:1; Rare:65 | ||||
| chr4:57008725-57008971 | Common:2; Rare:44 | ||||
| chr4:57016785-57017109 | Common:3; Rare:64 | ||||
| chr4:57033178-57033470 | Common:1; Rare:74 | ||||
| chr4:57078508-57078576 | Rare:10 | ||||
| chr4:57084523-57084732 | Common:3; Rare:26 | ||||
| chr4:57101667-57101857 | Rare:37 | ||||
| chr4:57104465-57104758 | Common:3; Rare:55 | ||||
| chr4:59748202-59748367 | Common:3; Rare:20 | ||||
| chr4:67415913-67415984 | Common:1; Rare:5 | ||||
| chr4:67509967-67510240 | Rare:42 | ||||
| chr4:67622865-67623227 | Rare:82 | ||||
| chr4:67628330-67628353 | Rare:4 |