| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10115520-10115748 | Common:3; Rare:82 | ||||
| chr3:10505468-10505799 | Common:2; Rare:61 | ||||
| chr3:11720705-11720867 | Rare:27 | ||||
| chr3:12288918-12289067 | Rare:33 | ||||
| chr3:12664056-12664351 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13480029-13480339 | Common:2; Rare:75 | ||||
| chr3:14124665-14125105 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178524-14178880 | Common:2; Rare:184; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651486-14651807 | Rare:93 | ||||
| chr3:14947226-14947554 | Common:4; Rare:148 | ||||
| chr3:15065067-15065161 | Rare:31 | ||||
| chr3:15065168-15065389 | Common:2; Rare:82 | ||||
| chr3:15099128-15099299 | Rare:43 | ||||
| chr3:15205976-15206290 | Common:1; Rare:117 | ||||
| chr3:15427471-15427635 | Common:1; Rare:60 |