| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13480060-13480339 | Common:1; Rare:66 | ||||
| chr3:13548982-13549177 | Common:1; Rare:63 | ||||
| chr3:14124729-14125184 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178881 | Common:2; Rare:169; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402415-14402700 | Common:1; Rare:71 | ||||
| chr3:14651423-14651847 | Common:1; Rare:132 | ||||
| chr3:14947372-14947554 | Common:3; Rare:89 | ||||
| chr3:15065226-15065498 | Common:5; Rare:87 | ||||
| chr3:15099128-15099293 | Rare:40 | ||||
| chr3:15205963-15206269 | Rare:110 | ||||
| chr3:15427478-15427645 | Common:1; Rare:58 | ||||
| chr3:15601516-15601804 | Common:4; Rare:121; Clinvar:1 | ||||
| chr3:16264866-16265225 | Common:2; Rare:120 | ||||
| chr3:16513592-16513873 | Common:4; Rare:74 | ||||
| chr3:17742591-17742952 | Common:4; Rare:127 |