| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75990848-75991061 | Common:1; Rare:83 | ||||
| chr4:76148366-76148577 | Common:3; Rare:66 | ||||
| chr4:76213532-76214014 | Common:4; Rare:167; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:76251582-76251747 | Rare:39 | ||||
| chr4:76306234-76306301 | Common:1; Rare:12 | ||||
| chr4:76306520-76306767 | Common:1; Rare:69 | ||||
| chr4:76586007-76586306 | Common:3; Rare:57 | ||||
| chr4:76949559-76949884 | Common:2; Rare:108 | ||||
| chr4:77075961-77076117 | Common:3; Rare:80 | ||||
| chr4:77076278-77076397 | Common:3; Rare:62 | ||||
| chr4:77157964-77158175 | Common:1; Rare:75 | ||||
| chr4:77862641-77862861 | Common:3; Rare:75 | ||||
| chr4:80072525-80072901 | Common:3; Rare:107; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:80073030-80073267 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:80183705-80183941 | Common:3; Rare:57 |