| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:106315550-106315586 | Rare:7 | ||||
| chr4:106316161-106316948 | Common:6; Rare:208 | ||||
| chr4:107720110-107720524 | Common:9; Rare:167 | ||||
| chr4:107824284-107824594 | Common:2; Rare:53 | ||||
| chr4:107824714-107825053 | Common:1; Rare:91 | ||||
| chr4:107931844-107932099 | Rare:87; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr4:107989746-107990053 | Common:4; Rare:132; Clinvar:4; Clinvar (benign):4 | ||||
| chr4:108620384-108620671 | Common:6; Rare:141 | ||||
| chr4:108650552-108650791 | Rare:82 | ||||
| chr4:109433753-109433998 | Common:1; Rare:86 | ||||
| chr4:109560133-109560424 | Rare:90 | ||||
| chr4:109560968-109560990 | Rare:9 | ||||
| chr4:109703362-109703550 | Rare:71 | ||||
| chr4:109730028-109730240 | Common:3; Rare:54 | ||||
| chr4:109815380-109815980 | Common:2; Rare:147 |