| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:13627717-13627877 | Common:1; Rare:47 | ||||
| chr4:15002293-15002505 | Common:1; Rare:74 | ||||
| chr4:15469787-15469903 | Common:1; Rare:24 | ||||
| chr4:15479456-15479535 | Common:1; Rare:14 | ||||
| chr4:15655295-15655499 | Common:1; Rare:93 | ||||
| chr4:15681457-15681901 | Common:4; Rare:154 | ||||
| chr4:16083678-16083881 | Common:2; Rare:60 | ||||
| chr4:17512055-17512307 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:17577350-17577566 | Rare:107 | ||||
| chr4:17614537-17614670 | Common:2; Rare:60 | ||||
| chr4:17810546-17811161 | Common:5; Rare:179 | ||||
| chr4:18021608-18021793 | Rare:96 | ||||
| chr4:20252758-20252891 | Common:1; Rare:30 | ||||
| chr4:20253352-20253521 | Common:2; Rare:36 | ||||
| chr4:20700239-20700502 | Common:1; Rare:114 |