| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10321054-10321279 | Common:2; Rare:88 | ||||
| chr3:11272227-11272427 | Common:1; Rare:44 | ||||
| chr3:11582334-11582466 | Rare:42 | ||||
| chr3:11643817-11644016 | Common:2; Rare:59 | ||||
| chr3:12484328-12484517 | Common:4; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12664084-12664310 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13420208-13420458 | Common:1; Rare:74 | ||||
| chr3:14124746-14125045 | Common:3; Rare:86; Clinvar:3 | ||||
| chr3:14178549-14178876 | Common:2; Rare:170; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402435-14402653 | Rare:55 | ||||
| chr3:14651468-14651818 | Rare:104 | ||||
| chr3:14947412-14947563 | Common:2; Rare:74 | ||||
| chr3:14948363-14948703 | Common:2; Rare:111 | ||||
| chr3:15065274-15065389 | Common:2; Rare:35 | ||||
| chr3:15099128-15099299 | Rare:43 |