| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32534205-32534366 | Common:2; Rare:31 | ||||
| chr12:32679050-32679358 | Common:4; Rare:233; Clinvar:1; Clinvar (benign):7 | ||||
| chr12:32755090-32755450 | Common:2; Rare:210; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr12:32755849-32756017 | Rare:123 | ||||
| chr12:32896727-32897023 | Common:7; Rare:181; Clinvar:8; Clinvar (benign):12 | ||||
| chr12:38905575-38905756 | Common:7; Rare:86 | ||||
| chr12:39443100-39443487 | Common:4; Rare:227; Clinvar:16; Clinvar (benign):10 | ||||
| chr12:40106013-40106266 | Common:1; Rare:96 | ||||
| chr12:42144640-42145023 | Common:14; Rare:290 | ||||
| chr12:42238175-42238433 | Common:2; Rare:156 | ||||
| chr12:42326030-42326227 | Common:2; Rare:116 | ||||
| chr12:43758702-43759021 | Common:4; Rare:179; Clinvar:4 | ||||
| chr12:45215390-45215671 | Common:1; Rare:76 | ||||
| chr12:45215862-45216291 | Common:6; Rare:225 | ||||
| chr12:45729559-45729943 | Common:2; Rare:199; Clinvar:2 |