| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62260220-62260564 | Rare:123 | ||||
| chr12:62260745-62260820 | Rare:22 | ||||
| chr12:62466596-62466971 | Common:1; Rare:104 | ||||
| chr12:62466976-62467066 | Common:1; Rare:13 | ||||
| chr12:62467207-62467372 | Common:1; Rare:49 | ||||
| chr12:62934329-62934463 | Common:1; Rare:29 | ||||
| chr12:62934588-62934770 | Rare:66 | ||||
| chr12:62934880-62934969 | Rare:14 | ||||
| chr12:62935055-62935351 | Common:1; Rare:75 | ||||
| chr12:63151077-63151380 | Common:1; Rare:63 | ||||
| chr12:63779715-63779957 | Common:3; Rare:88; Clinvar (benign):1 | ||||
| chr12:63780008-63780472 | Common:1; Rare:151; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr12:63843789-63844437 | Common:7; Rare:138 | ||||
| chr12:63844445-63844772 | Rare:77 | ||||
| chr12:63844999-63845141 | Rare:25 |