| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10115520-10115802 | Common:3; Rare:89 | ||||
| chr3:11225863-11226020 | Rare:24 | ||||
| chr3:12158752-12158799 | Rare:29 | ||||
| chr3:12484333-12484529 | Common:5; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:13568841-13568992 | Common:1; Rare:29 | ||||
| chr3:14124703-14125156 | Common:4; Rare:134; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178549-14178862 | Common:2; Rare:163; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651480-14651813 | Rare:98 | ||||
| chr3:14947213-14947803 | Common:7; Rare:254 | ||||
| chr3:15427460-15427621 | Common:1; Rare:61 | ||||
| chr3:15601456-15601760 | Common:4; Rare:121 | ||||
| chr3:15797274-15797442 | Rare:28 | ||||
| chr3:15859777-15860098 | Common:4; Rare:97 | ||||
| chr3:16264787-16265247 | Common:3; Rare:160 | ||||
| chr3:19946905-19947250 | Common:6; Rare:122 |