| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4275444-4275590 | Common:2; Rare:22 | ||||
| chr12:4320943-4321260 | Common:5; Rare:121 | ||||
| chr12:4538444-4538907 | Common:1; Rare:102 | ||||
| chr12:4649045-4649164 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr12:5043929-5044036 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chr12:6124569-6124934 | Rare:46 | ||||
| chr12:6200005-6200485 | Common:4; Rare:138 | ||||
| chr12:6200678-6200794 | Common:1; Rare:17 | ||||
| chr12:6330660-6330886 | Common:1; Rare:66; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:6341919-6342406 | Common:2; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:6383980-6384262 | Common:1; Rare:63 | ||||
| chr12:6452070-6452128 | Common:1; Rare:15 | ||||
| chr12:6470660-6470898 | Rare:64 | ||||
| chr12:6493117-6493386 | Common:7; Rare:84 | ||||
| chr12:6493734-6493975 | Common:2; Rare:74 |