| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32570747-32571206 | Common:3; Rare:156 | ||||
| chr3:33097094-33097258 | Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277295-33277482 | Common:2; Rare:49 | ||||
| chr3:33718071-33718314 | Rare:93 | ||||
| chr3:33798495-33798639 | Common:2; Rare:43 | ||||
| chr3:36993073-36993559 | Common:2; Rare:165; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:36993663-36993826 | Rare:67; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37243166-37243310 | Common:1; Rare:34 | ||||
| chr3:38029605-38029924 | Common:2; Rare:61 | ||||
| chr3:39051899-39052050 | Common:1; Rare:50 | ||||
| chr3:39107606-39107735 | Common:3; Rare:34 | ||||
| chr3:39383289-39383437 | Common:2; Rare:24; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383518-39383653 | Rare:29; Clinvar:1 | ||||
| chr3:39406514-39406750 | Common:6; Rare:102 | ||||
| chr3:40309446-40309803 | Common:9; Rare:122 |