| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64826160-64826510 | Common:2; Rare:59 | ||||
| chr12:64875546-64876215 | Common:4; Rare:231 | ||||
| chr12:64877280-64877670 | Common:1; Rare:70 | ||||
| chr12:64882758-64882915 | Rare:43 | ||||
| chr12:64883197-64883817 | Common:4; Rare:249 | ||||
| chr12:64884000-64884330 | Common:5; Rare:64 | ||||
| chr12:64884764-64885220 | Rare:102 | ||||
| chr12:64886078-64886478 | Common:2; Rare:64 | ||||
| chr12:65156410-65156770 | Common:2; Rare:85 | ||||
| chr12:65170127-65170602 | Common:1; Rare:196; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr12:65188420-65188890 | Common:3; Rare:97 | ||||
| chr12:65536992-65537392 | Common:5; Rare:95 | ||||
| chr12:65741280-65741750 | Common:13; Rare:115 | ||||
| chr12:65881390-65881880 | Common:1; Rare:120 | ||||
| chr12:65881900-65882510 | Common:4; Rare:210 |