| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7129957-7130014 | Rare:8 | ||||
| chr12:7130193-7130441 | Common:5; Rare:62 | ||||
| chr12:7131221-7131435 | Common:1; Rare:37 | ||||
| chr12:7189502-7189774 | Common:2; Rare:94; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:7189916-7189970 | Common:1; Rare:18; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:7711424-7711444 | Rare:2 | ||||
| chr12:7711460-7711479 | Rare:4 | ||||
| chr12:7711487-7711815 | Common:3; Rare:90 | ||||
| chr12:7832334-7832364 | Common:1; Rare:3 | ||||
| chr12:7890682-7890887 | Common:1; Rare:46 | ||||
| chr12:7891079-7891135 | Common:1; Rare:13 | ||||
| chr12:7891144-7891205 | Rare:17 | ||||
| chr12:7935850-7935936 | Common:1; Rare:18 | ||||
| chr12:7936025-7936475 | Common:5; Rare:68 | ||||
| chr12:8032512-8032830 | Common:5; Rare:96 |