| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:156774054-156774186 | Rare:21 | ||||
| chr4:156970957-156971215 | Rare:37 | ||||
| chr4:158172347-158172736 | Rare:65 | ||||
| chr4:158671731-158672389 | Common:6; Rare:175; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723208-158723439 | Common:2; Rare:101 | ||||
| chr4:159229228-159229578 | Common:2; Rare:59 | ||||
| chr4:163166363-163166440 | Common:1; Rare:39 | ||||
| chr4:163166818-163167024 | Common:2; Rare:77 | ||||
| chr4:163494488-163494807 | Common:3; Rare:126 | ||||
| chr4:164977553-164977695 | Rare:39 | ||||
| chr4:165112786-165113013 | Common:1; Rare:75 | ||||
| chr4:165327354-165327748 | Common:3; Rare:122 | ||||
| chr4:168318739-168318881 | Rare:30 | ||||
| chr4:168480399-168480496 | Common:1; Rare:20 | ||||
| chr4:168921530-168921892 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):1 |