| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50283477-50283672 | Common:3; Rare:62 | ||||
| chr12:50400693-50401016 | Common:1; Rare:106 | ||||
| chr12:50504858-50505138 | Common:4; Rare:114 | ||||
| chr12:50763948-50764326 | Common:1; Rare:100 | ||||
| chr12:50764348-50764501 | Common:2; Rare:49 | ||||
| chr12:51009145-51009327 | Common:1; Rare:34 | ||||
| chr12:51025155-51025245 | Rare:20 | ||||
| chr12:51025727-51025943 | Common:1; Rare:47 | ||||
| chr12:51026313-51026542 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048057-51048359 | Common:2; Rare:99 | ||||
| chr12:51172769-51172904 | Common:2; Rare:32 | ||||
| chr12:51173067-51173191 | Rare:23 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51270365-51270427 | Rare:18 | ||||
| chr12:51590717-51590933 | Common:1; Rare:62 |