| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158172360-158172734 | Rare:61 | ||||
| chr4:158172986-158173218 | Rare:36 | ||||
| chr4:158210352-158210528 | Common:2; Rare:36 | ||||
| chr4:158671849-158672427 | Common:5; Rare:152; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723319-158723480 | Common:2; Rare:74 | ||||
| chr4:159267051-159267185 | Rare:20 | ||||
| chr4:162163938-162164125 | Rare:43 | ||||
| chr4:163166879-163167096 | Common:2; Rare:75 | ||||
| chr4:164383941-164384144 | Common:1; Rare:43 | ||||
| chr4:164977607-164977727 | Rare:32 | ||||
| chr4:165112825-165113015 | Common:1; Rare:56 | ||||
| chr4:165327346-165327776 | Common:3; Rare:132 | ||||
| chr4:165378732-165378849 | Rare:25 | ||||
| chr4:168480468-168480556 | Rare:17 | ||||
| chr4:168631497-168631655 | Rare:45 |