| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52038240-52038346 | Rare:45; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659192-52659402 | Common:1; Rare:72 | ||||
| chr4:53366017-53366134 | Rare:22 | ||||
| chr4:55395852-55395957 | Common:1; Rare:28; Clinvar:2 | ||||
| chr4:55546602-55546739 | Common:4; Rare:23 | ||||
| chr4:55546814-55547012 | Common:2; Rare:68 | ||||
| chr4:55547085-55547162 | Rare:27 | ||||
| chr4:55853476-55853784 | Rare:85 | ||||
| chr4:56387423-56387524 | Rare:35 | ||||
| chr4:56435473-56435973 | Common:6; Rare:164 | ||||
| chr4:56435997-56436321 | Rare:114 | ||||
| chr4:56467495-56467645 | Rare:59 | ||||
| chr4:56681282-56681498 | Common:1; Rare:29 | ||||
| chr4:56977574-56977753 | Common:1; Rare:71 | ||||
| chr4:67545442-67545742 | Common:2; Rare:76 |