| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50222155-50222555 | Rare:152 | ||||
| chr12:50283473-50283744 | Common:4; Rare:84 | ||||
| chr12:50400675-50401005 | Common:1; Rare:101 | ||||
| chr12:50504821-50505120 | Common:3; Rare:119 | ||||
| chr12:50505490-50505930 | Common:4; Rare:106 | ||||
| chr12:50763286-50763703 | Common:11; Rare:100 | ||||
| chr12:50763882-50764131 | Common:2; Rare:75 | ||||
| chr12:50764386-50764516 | Common:4; Rare:43 | ||||
| chr12:50924387-50924787 | Common:3; Rare:116 | ||||
| chr12:51025729-51025946 | Common:1; Rare:49 | ||||
| chr12:51026317-51026515 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51047835-51047966 | Common:1; Rare:17 | ||||
| chr12:51048088-51048411 | Common:2; Rare:115 | ||||
| chr12:51083521-51083792 | Common:1; Rare:108 | ||||
| chr12:51172695-51172940 | Common:3; Rare:50 |