| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56467526-56467699 | Common:2; Rare:72; Clinvar (benign):5 | ||||
| chr4:56500454-56500652 | Rare:62; Clinvar (benign):2 | ||||
| chr4:56680818-56681110 | Rare:53 | ||||
| chr4:56977597-56977732 | Common:1; Rare:48 | ||||
| chr4:67545351-67545748 | Common:2; Rare:99 | ||||
| chr4:67701111-67701358 | Common:4; Rare:118 | ||||
| chr4:68349932-68350228 | Common:2; Rare:103 | ||||
| chr4:69860101-69860285 | Common:1; Rare:32 | ||||
| chr4:70688345-70688587 | Common:2; Rare:62 | ||||
| chr4:70993482-70993661 | Common:4; Rare:53 | ||||
| chr4:73069707-73069892 | Common:1; Rare:78 | ||||
| chr4:73258469-73258913 | Common:1; Rare:133 | ||||
| chr4:74099191-74099406 | Common:2; Rare:52 | ||||
| chr4:74157923-74158188 | Common:1; Rare:122 | ||||
| chr4:74444940-74445156 | Common:1; Rare:39 |