| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:76305927-76306080 | Common:1; Rare:21 | ||||
| chr4:76306476-76306915 | Common:2; Rare:137 | ||||
| chr4:76949618-76949922 | Common:1; Rare:93 | ||||
| chr4:76987293-76987647 | Rare:61 | ||||
| chr4:77034358-77034591 | Rare:40 | ||||
| chr4:77075473-77075530 | Rare:26 | ||||
| chr4:77075942-77076107 | Common:3; Rare:91 | ||||
| chr4:77076292-77076413 | Common:2; Rare:59 | ||||
| chr4:77157107-77157361 | Common:6; Rare:107 | ||||
| chr4:77862632-77862917 | Common:3; Rare:114 | ||||
| chr4:78939348-78939555 | Common:2; Rare:104 | ||||
| chr4:80072142-80072309 | Common:2; Rare:40 | ||||
| chr4:80072555-80072800 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:80073193-80073482 | Common:1; Rare:74; Clinvar:1 | ||||
| chr4:80184097-80184325 | Rare:59 |