| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804242-42804756 | Common:3; Rare:146 | ||||
| chr3:43286449-43286664 | Common:2; Rare:93 | ||||
| chr3:43621899-43622322 | Common:2; Rare:123; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690787-43691004 | Common:3; Rare:118; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691544-43691643 | Common:1; Rare:17 | ||||
| chr3:44338327-44338804 | Common:8; Rare:157 | ||||
| chr3:44477625-44477746 | Common:1; Rare:27 | ||||
| chr3:44510581-44510666 | Common:2; Rare:25 | ||||
| chr3:44584715-44584981 | Rare:49 | ||||
| chr3:44624935-44625106 | Common:2; Rare:49 | ||||
| chr3:44648544-44648810 | Rare:60 | ||||
| chr3:44729537-44729687 | Common:1; Rare:56 | ||||
| chr3:44761529-44761817 | Common:3; Rare:121 | ||||
| chr3:44861796-44861939 | Common:2; Rare:68 | ||||
| chr3:44976064-44976317 | Common:3; Rare:105 |