| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42773055-42773455 | Common:6; Rare:201 | ||||
| chr3:42803868-42804075 | Common:2; Rare:64 | ||||
| chr3:42804133-42804809 | Common:10; Rare:415 | ||||
| chr3:42979400-42980030 | Common:5; Rare:231 | ||||
| chr3:43105742-43105847 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr3:43105951-43106155 | Common:3; Rare:80 | ||||
| chr3:43286282-43286662 | Common:6; Rare:305 | ||||
| chr3:43621833-43622490 | Common:6; Rare:441; Clinvar:21; Clinvar (benign):3 | ||||
| chr3:43690585-43691089 | Common:16; Rare:466; Clinvar:23; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr3:43691432-43691800 | Common:4; Rare:145 | ||||
| chr3:44338018-44338606 | Common:17; Rare:444 | ||||
| chr3:44338590-44338856 | Common:9; Rare:168 | ||||
| chr3:44477132-44477532 | Common:2; Rare:182 | ||||
| chr3:44477583-44477696 | Rare:37 | ||||
| chr3:44477613-44477775 | Common:2; Rare:70 |