| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:59596231-59596438 | Common:2; Rare:50 | ||||
| chr12:59596480-59596790 | Common:6; Rare:62 | ||||
| chr12:59596870-59597166 | Common:2; Rare:70 | ||||
| chr12:59597443-59597712 | Common:3; Rare:43 | ||||
| chr12:62259349-62259398 | Rare:8 | ||||
| chr12:62259401-62259501 | Rare:18 | ||||
| chr12:62259663-62260229 | Common:1; Rare:164 | ||||
| chr12:62260237-62260520 | Rare:101 | ||||
| chr12:62260765-62261152 | Rare:95 | ||||
| chr12:62466200-62466334 | Rare:25 | ||||
| chr12:62466568-62466925 | Rare:100 | ||||
| chr12:63779685-63779958 | Common:3; Rare:99; Clinvar (benign):1 | ||||
| chr12:63780054-63780350 | Rare:106; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:63843857-63844117 | Common:5; Rare:60 | ||||
| chr12:64221772-64221892 | Rare:26 |