| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64451739-64451929 | Rare:53 | ||||
| chr12:64451964-64452349 | Common:1; Rare:135 | ||||
| chr12:64452476-64452559 | Rare:19 | ||||
| chr12:64452891-64453041 | Common:1; Rare:33 | ||||
| chr12:64610113-64610548 | Common:6; Rare:139 | ||||
| chr12:64610906-64611040 | Rare:28 | ||||
| chr12:64758868-64759114 | Rare:67 | ||||
| chr12:64759335-64759683 | Common:3; Rare:103; Clinvar:3 | ||||
| chr12:64780480-64780716 | Common:2; Rare:56 | ||||
| chr12:64781163-64781239 | Rare:18 | ||||
| chr12:64781345-64781451 | Rare:19 | ||||
| chr12:64824499-64824622 | Common:2; Rare:36 | ||||
| chr12:65169312-65169648 | Common:1; Rare:114; Clinvar:2 | ||||
| chr12:65278607-65279047 | Common:1; Rare:134; Clinvar (benign):4 | ||||
| chr12:65823492-65823646 | Common:1; Rare:31 |