| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74444921-74445406 | Common:5; Rare:114 | ||||
| chr4:75514273-75514505 | Common:1; Rare:80 | ||||
| chr4:75514707-75514766 | Rare:13 | ||||
| chr4:75630493-75630668 | Rare:42 | ||||
| chr4:75673250-75673712 | Common:1; Rare:177 | ||||
| chr4:75724412-75724810 | Common:2; Rare:125 | ||||
| chr4:75990892-75990972 | Rare:33 | ||||
| chr4:76148366-76148581 | Common:4; Rare:67 | ||||
| chr4:76213462-76213531 | Common:1; Rare:17; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:76213534-76214005 | Common:4; Rare:163; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:76251667-76251759 | Rare:27 | ||||
| chr4:76586110-76586306 | Common:2; Rare:33 | ||||
| chr4:76949559-76949930 | Common:2; Rare:122 | ||||
| chr4:76987536-76987714 | Rare:33 | ||||
| chr4:77028459-77028758 | Common:2; Rare:55 |