| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75673291-75673675 | Common:1; Rare:153 | ||||
| chr4:75724374-75724714 | Common:1; Rare:93 | ||||
| chr4:76148357-76148577 | Common:3; Rare:70 | ||||
| chr4:76213654-76214014 | Common:2; Rare:114 | ||||
| chr4:76251667-76251749 | Rare:24 | ||||
| chr4:76434928-76435255 | Common:4; Rare:58 | ||||
| chr4:76435500-76435559 | Common:1; Rare:10 | ||||
| chr4:76436101-76436123 | Rare:9 | ||||
| chr4:76949569-76949879 | Common:2; Rare:101 | ||||
| chr4:77075557-77075757 | Common:2; Rare:80 | ||||
| chr4:77075967-77076090 | Common:3; Rare:63 | ||||
| chr4:77862643-77862879 | Common:3; Rare:89 | ||||
| chr4:78057462-78057604 | Common:2; Rare:32 | ||||
| chr4:78939246-78939519 | Common:2; Rare:115 | ||||
| chr4:80073069-80073190 | Common:1; Rare:29; Clinvar (benign):1 |