| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:6693697-6693888 | Rare:42 | ||||
| chr4:6709825-6709982 | Common:1; Rare:46 | ||||
| chr4:6987006-6987276 | Common:2; Rare:80 | ||||
| chr4:7068007-7068373 | Common:6; Rare:128 | ||||
| chr4:8440702-8440807 | Rare:42 | ||||
| chr4:10116717-10117047 | Common:6; Rare:152 | ||||
| chr4:15427942-15428065 | Rare:14 | ||||
| chr4:15478971-15479237 | Common:2; Rare:52 | ||||
| chr4:15655262-15655459 | Common:2; Rare:83 | ||||
| chr4:17577316-17577549 | Rare:110 | ||||
| chr4:17614555-17614651 | Common:2; Rare:40 | ||||
| chr4:17810681-17810873 | Rare:61 | ||||
| chr4:18021732-18021990 | Common:2; Rare:88 | ||||
| chr4:20700322-20700493 | Common:1; Rare:73 | ||||
| chr4:25160380-25160733 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):1 |