| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:58920496-58920681 | Common:2; Rare:67 | ||||
| chr12:59595772-59596176 | Common:7; Rare:91 | ||||
| chr12:62192716-62192815 | Common:1; Rare:24 | ||||
| chr12:62259710-62259830 | Rare:27 | ||||
| chr12:62260051-62260460 | Common:1; Rare:152 | ||||
| chr12:62278488-62278656 | Rare:30 | ||||
| chr12:62279162-62279302 | Common:1; Rare:15 | ||||
| chr12:62355181-62355426 | Common:1; Rare:50 | ||||
| chr12:62466680-62466926 | Rare:73 | ||||
| chr12:63569306-63569440 | Rare:29; Clinvar (pathogenic):1 | ||||
| chr12:63584648-63584774 | Common:1; Rare:10 | ||||
| chr12:63668444-63668709 | Common:3; Rare:73 | ||||
| chr12:63668751-63669060 | Common:4; Rare:65 | ||||
| chr12:63779720-63779917 | Common:3; Rare:70 | ||||
| chr12:63780065-63780175 | Rare:53; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 |