| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52407257-52407434 | Rare:48; Clinvar:4; Clinvar (benign):7 | ||||
| chr3:53236253-53236413 | Common:2; Rare:29 | ||||
| chr3:54355955-54356153 | Common:1; Rare:38 | ||||
| chr3:57805771-57805948 | Common:1; Rare:35 | ||||
| chr3:57952293-57952380 | Rare:14 | ||||
| chr3:57983405-57983569 | Common:2; Rare:27 | ||||
| chr3:58350854-58350874 | Common:1; Rare:5 | ||||
| chr3:61560712-61560828 | Common:1; Rare:37 | ||||
| chr3:61743132-61743140 | Rare:2 | ||||
| chr3:75432865-75433135 | Common:4; Rare:51 | ||||
| chr3:75434083-75434401 | Common:10; Rare:57 | ||||
| chr3:75434992-75435388 | Common:6; Rare:133 | ||||
| chr3:81761002-81761319 | Rare:87 | ||||
| chr3:84191074-84191123 | Rare:15 | ||||
| chr3:94064323-94064659 | Rare:83 |