| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:78056719-78056782 | Rare:11 | ||||
| chr4:78638439-78638647 | Common:1; Rare:26 | ||||
| chr4:78707284-78707489 | Common:2; Rare:30 | ||||
| chr4:78721157-78721329 | Common:2; Rare:31 | ||||
| chr4:78737077-78737127 | Rare:5 | ||||
| chr4:78750259-78750611 | Common:1; Rare:58 | ||||
| chr4:78775415-78775590 | Common:1; Rare:47 | ||||
| chr4:78777042-78777142 | Rare:13 | ||||
| chr4:80139036-80139149 | Rare:15 | ||||
| chr4:80203295-80203385 | Rare:23; Clinvar (benign):1 | ||||
| chr4:81470483-81470576 | Common:1; Rare:23 | ||||
| chr4:81473150-81473167 | Rare:6 | ||||
| chr4:81506904-81507097 | Common:5; Rare:30 | ||||
| chr4:81562211-81562479 | Common:3; Rare:51 | ||||
| chr4:81565626-81565716 | Rare:17 |