| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63779719-63779964 | Common:3; Rare:88; Clinvar (benign):1 | ||||
| chr12:63779996-63780244 | Common:1; Rare:113; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr12:63780283-63780396 | Rare:19 | ||||
| chr12:63843862-63844101 | Common:4; Rare:56 | ||||
| chr12:63844468-63844724 | Rare:64 | ||||
| chr12:63845112-63845176 | Rare:10 | ||||
| chr12:64042911-64043008 | Rare:19 | ||||
| chr12:64043021-64043151 | Common:1; Rare:22 | ||||
| chr12:64221776-64222040 | Rare:53 | ||||
| chr12:64222203-64222426 | Common:1; Rare:81 | ||||
| chr12:64222461-64222626 | Rare:27 | ||||
| chr12:64404016-64404777 | Common:8; Rare:236 | ||||
| chr12:64404843-64405247 | Common:1; Rare:94 | ||||
| chr12:64405272-64405376 | Rare:15 | ||||
| chr12:64451815-64452337 | Common:2; Rare:172 |