| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63780080-63780159 | Rare:32; Clinvar (pathogenic):1 | ||||
| chr12:63844652-63844879 | Common:1; Rare:64 | ||||
| chr12:64222230-64222366 | Rare:48 | ||||
| chr12:64404227-64404639 | Common:5; Rare:150 | ||||
| chr12:64404698-64404754 | Rare:19 | ||||
| chr12:64451683-64452182 | Common:2; Rare:154 | ||||
| chr12:64610156-64610495 | Common:5; Rare:109 | ||||
| chr12:64759309-64759501 | Common:1; Rare:60; Clinvar:3 | ||||
| chr12:65169411-65169644 | Common:1; Rare:85; Clinvar:2 | ||||
| chr12:65823504-65823648 | Common:1; Rare:29 | ||||
| chr12:65824129-65824264 | Rare:39 | ||||
| chr12:65824283-65824700 | Common:1; Rare:99 | ||||
| chr12:65824749-65825326 | Common:1; Rare:140 | ||||
| chr12:65825337-65825404 | Rare:7 | ||||
| chr12:66130700-66130821 | Rare:44 |