| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55395815-55395994 | Common:2; Rare:52; Clinvar:2 | ||||
| chr4:55396308-55396393 | Rare:25; Clinvar (benign):1 | ||||
| chr4:55546494-55546540 | Rare:11 | ||||
| chr4:55546652-55546959 | Common:4; Rare:97 | ||||
| chr4:55547085-55547199 | Common:1; Rare:42 | ||||
| chr4:55853483-55853801 | Rare:91 | ||||
| chr4:56048888-56049158 | Common:3; Rare:78 | ||||
| chr4:56387384-56387574 | Rare:68 | ||||
| chr4:56435436-56436355 | Common:6; Rare:310 | ||||
| chr4:56467524-56467735 | Common:2; Rare:84; Clinvar (benign):5 | ||||
| chr4:56500429-56500646 | Rare:65; Clinvar (benign):2 | ||||
| chr4:56821658-56821808 | Common:6; Rare:55 | ||||
| chr4:56907550-56907983 | Common:4; Rare:141 | ||||
| chr4:56908341-56908744 | Common:2; Rare:105 | ||||
| chr4:56977537-56977787 | Common:2; Rare:93 |