| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:30720228-30720425 | Common:1; Rare:54 | ||||
| chr4:30723580-30723778 | Rare:49 | ||||
| chr4:30724153-30724391 | Common:1; Rare:67 | ||||
| chr4:37826510-37826729 | Common:6; Rare:79 | ||||
| chr4:39458834-39459112 | Common:3; Rare:153; Clinvar (benign):5 | ||||
| chr4:39527323-39527746 | Common:4; Rare:105 | ||||
| chr4:39527952-39528021 | Rare:18 | ||||
| chr4:39638825-39639169 | Common:1; Rare:123 | ||||
| chr4:39697966-39698375 | Common:1; Rare:137 | ||||
| chr4:41256826-41257008 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41990690-41990757 | Common:1; Rare:24 | ||||
| chr4:44678400-44678680 | Common:1; Rare:106 | ||||
| chr4:44726481-44726633 | Common:2; Rare:54 | ||||
| chr4:46993528-46993680 | Common:2; Rare:42 | ||||
| chr4:51842808-51843239 | Common:1; Rare:131 |