| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:22625787-22626187 | Common:1; Rare:84 | ||||
| chr12:23949547-23949977 | Common:15; Rare:189 | ||||
| chr12:23950125-23950613 | Common:7; Rare:190 | ||||
| chr12:24948299-24948699 | Common:4; Rare:88 | ||||
| chr12:24948950-24949483 | Common:19; Rare:543 | ||||
| chr12:24949440-24949840 | Rare:59 | ||||
| chr12:25051610-25052010 | Common:2; Rare:62 | ||||
| chr12:25052020-25052830 | Common:15; Rare:283 | ||||
| chr12:25052834-25053234 | Common:1; Rare:85 | ||||
| chr12:25195008-25195686 | Common:18; Rare:584 | ||||
| chr12:25250326-25250927 | Common:8; Rare:234; Clinvar:5; Clinvar (benign):8 | ||||
| chr12:25250836-25251620 | Common:3; Rare:727; Clinvar:17; Clinvar (benign):13 | ||||
| chr12:25958350-25958950 | Common:13; Rare:685 | ||||
| chr12:26832420-26832570 | Common:1; Rare:58 | ||||
| chr12:26833060-26833557 | Common:9; Rare:507 |