| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827440-102827611 | Rare:63 | ||||
| chr4:102827762-102827942 | Common:1; Rare:59 | ||||
| chr4:102868819-102869066 | Common:2; Rare:84 | ||||
| chr4:105146571-105146887 | Common:2; Rare:105 | ||||
| chr4:105708633-105708830 | Rare:63 | ||||
| chr4:106315558-106315582 | Rare:6 | ||||
| chr4:106316154-106316933 | Common:6; Rare:208 | ||||
| chr4:107720110-107720499 | Common:9; Rare:157 | ||||
| chr4:107989690-107989942 | Common:5; Rare:112; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620391-108620709 | Common:6; Rare:144 | ||||
| chr4:108621950-108622204 | Common:1; Rare:62 | ||||
| chr4:109433758-109433890 | Common:1; Rare:50 | ||||
| chr4:109560068-109560430 | Common:5; Rare:106 | ||||
| chr4:109730033-109730242 | Common:3; Rare:53 | ||||
| chr4:109815380-109815817 | Common:2; Rare:110 |