| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42633342-42633612 | Rare:52 | ||||
| chr3:42773187-42773345 | Common:1; Rare:47 | ||||
| chr3:42804272-42804671 | Common:2; Rare:112 | ||||
| chr3:43621968-43622322 | Common:2; Rare:97; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:43690817-43690950 | Common:1; Rare:60; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:43691562-43691623 | Common:1; Rare:11 | ||||
| chr3:44338319-44338458 | Common:2; Rare:48 | ||||
| chr3:44338675-44338807 | Common:3; Rare:48 | ||||
| chr3:44477646-44477746 | Common:1; Rare:18 | ||||
| chr3:44584703-44584992 | Rare:52 | ||||
| chr3:44624851-44625033 | Common:1; Rare:46 | ||||
| chr3:44648721-44648804 | Rare:25 | ||||
| chr3:44729543-44729667 | Common:1; Rare:48 | ||||
| chr3:44761577-44761794 | Common:3; Rare:83 | ||||
| chr3:44861757-44861925 | Common:2; Rare:76 |