| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17810686-17811025 | Common:3; Rare:103 | ||||
| chr4:20700245-20700436 | Rare:79 | ||||
| chr4:24584473-24584719 | Common:1; Rare:77 | ||||
| chr4:25160386-25160731 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914058-25914283 | Common:2; Rare:95 | ||||
| chr4:38867693-38867814 | Common:1; Rare:52 | ||||
| chr4:39458857-39459121 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527405-39527729 | Common:2; Rare:78 | ||||
| chr4:39638859-39639140 | Common:1; Rare:105 | ||||
| chr4:39697936-39698174 | Common:2; Rare:103 | ||||
| chr4:44678369-44678683 | Common:1; Rare:115 | ||||
| chr4:44726534-44726642 | Rare:42 | ||||
| chr4:48016612-48016784 | Common:1; Rare:50 | ||||
| chr4:48780245-48780572 | Common:2; Rare:97 | ||||
| chr4:52038252-52038335 | Rare:33; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 |