| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11225823-11226036 | Rare:38 | ||||
| chr3:11719427-11719583 | Rare:49 | ||||
| chr3:12484333-12484517 | Common:4; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12664075-12664300 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480060-13480324 | Common:1; Rare:63 | ||||
| chr3:14124691-14125196 | Common:4; Rare:152; Clinvar:8; Clinvar (benign):2 | ||||
| chr3:14178565-14178867 | Common:2; Rare:157; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14947222-14947543 | Common:4; Rare:138 | ||||
| chr3:15065233-15065399 | Common:2; Rare:59 | ||||
| chr3:15205976-15206290 | Common:1; Rare:117 | ||||
| chr3:15427471-15427623 | Common:1; Rare:57 | ||||
| chr3:15601469-15601804 | Common:4; Rare:138; Clinvar:1 | ||||
| chr3:16264872-16265229 | Common:2; Rare:117 | ||||
| chr3:19946974-19947475 | Common:7; Rare:185 | ||||
| chr3:20186157-20186355 | Common:1; Rare:59 |