| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:389219-389371 | Rare:57 | ||||
| chr12:389375-389724 | Common:8; Rare:137 | ||||
| chr12:401383-401766 | Common:2; Rare:102 | ||||
| chr12:401785-401932 | Rare:26 | ||||
| chr12:459749-460222 | Common:3; Rare:142 | ||||
| chr12:642664-643555 | Common:11; Rare:241 | ||||
| chr12:643556-643661 | Rare:21 | ||||
| chr12:643856-643966 | Rare:25 | ||||
| chr12:752295-752752 | Common:1; Rare:140 | ||||
| chr12:752921-753201 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:949112-949342 | Rare:46 | ||||
| chr12:949348-950052 | Common:9; Rare:189 | ||||
| chr12:990395-990441 | Rare:6 | ||||
| chr12:990448-990591 | Common:1; Rare:40 | ||||
| chr12:990675-990927 | Rare:81 |