| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42739909-42740207 | Common:1; Rare:47 | ||||
| chr3:44833527-44833619 | Common:2; Rare:17 | ||||
| chr3:45113667-45113925 | Common:5; Rare:49 | ||||
| chr3:46858372-46858742 | Common:2; Rare:84; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr3:46860950-46861289 | Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:46861581-46861835 | Common:3; Rare:41 | ||||
| chr3:46864527-46864753 | Common:1; Rare:33 | ||||
| chr3:48425318-48425557 | Rare:56 | ||||
| chr3:48919900-48920113 | Common:2; Rare:34 | ||||
| chr3:48934493-48934740 | Rare:43 | ||||
| chr3:48948956-48949251 | Common:4; Rare:61 | ||||
| chr3:52235174-52235416 | Common:1; Rare:29 | ||||
| chr3:55572044-55572225 | Common:3; Rare:36 | ||||
| chr3:57252561-57252711 | Rare:16 | ||||
| chr3:61560894-61561037 | Common:2; Rare:39 |