| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42600281-42600741 | Common:3; Rare:177 | ||||
| chr3:42653950-42654650 | Common:2; Rare:166 | ||||
| chr3:42773181-42773372 | Common:1; Rare:55 | ||||
| chr3:42804415-42804710 | Common:2; Rare:98 | ||||
| chr3:43105760-43106320 | Common:5; Rare:164; Clinvar (benign):1 | ||||
| chr3:43286376-43286652 | Common:2; Rare:114 | ||||
| chr3:43621903-43622390 | Common:2; Rare:144; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690756-43691036 | Common:5; Rare:156; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691503-43691673 | Common:1; Rare:35 | ||||
| chr3:44338240-44338461 | Common:2; Rare:68 | ||||
| chr3:44338648-44338837 | Common:3; Rare:69 | ||||
| chr3:44338941-44339372 | Common:5; Rare:109 | ||||
| chr3:44477500-44477940 | Common:1; Rare:95 | ||||
| chr3:44510554-44510721 | Common:4; Rare:41 | ||||
| chr3:44555087-44555447 | Common:1; Rare:94 |