| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:24584375-24584840 | Common:6; Rare:663 | ||||
| chr4:24795224-24795624 | Common:4; Rare:213 | ||||
| chr4:24795960-24796310 | Common:5; Rare:55 | ||||
| chr4:24912950-24913230 | Common:4; Rare:85 | ||||
| chr4:25159840-25160240 | Common:5; Rare:182 | ||||
| chr4:25160267-25160784 | Common:29; Rare:1083; Clinvar:18; Clinvar (benign):9 | ||||
| chr4:25160756-25161156 | Common:13; Rare:91 | ||||
| chr4:25233496-25234115 | Common:3; Rare:701 | ||||
| chr4:25312471-25312876 | Common:7; Rare:345 | ||||
| chr4:25312892-25313292 | Common:2; Rare:78 | ||||
| chr4:25376870-25377402 | Common:25; Rare:849 | ||||
| chr4:25860839-25861239 | Common:3; Rare:153 | ||||
| chr4:25861444-25861844 | Common:9; Rare:134 | ||||
| chr4:25862000-25862360 | Common:4; Rare:121 | ||||
| chr4:25862760-25863360 | Common:2; Rare:110 |