| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42906044-42906158 | Common:2; Rare:31 | ||||
| chr3:43286459-43286654 | Common:2; Rare:86 | ||||
| chr3:43621919-43622326 | Common:2; Rare:119; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690634-43690993 | Common:6; Rare:152; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691548-43691685 | Common:1; Rare:24 | ||||
| chr3:44338373-44338800 | Common:6; Rare:144 | ||||
| chr3:44477625-44477746 | Common:1; Rare:27 | ||||
| chr3:44510601-44510796 | Common:3; Rare:49 | ||||
| chr3:44624836-44625118 | Common:3; Rare:75 | ||||
| chr3:44729506-44729667 | Common:1; Rare:62 | ||||
| chr3:44761583-44761829 | Common:3; Rare:90 | ||||
| chr3:44861767-44861925 | Common:2; Rare:71 | ||||
| chr3:44974969-44975278 | Common:3; Rare:43 | ||||
| chr3:44976091-44976289 | Common:2; Rare:82 | ||||
| chr3:45026060-45026368 | Common:3; Rare:64 |