| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120250133-120250277 | Rare:26 | ||||
| chr12:120437896-120438158 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:120446346-120446483 | Common:1; Rare:61 | ||||
| chr12:120469446-120469895 | Common:6; Rare:146 | ||||
| chr12:120495859-120496221 | Common:7; Rare:124 | ||||
| chr12:120529128-120529321 | Common:1; Rare:52 | ||||
| chr12:120581358-120581577 | Common:1; Rare:77 | ||||
| chr12:121802931-121803311 | Common:1; Rare:103 | ||||
| chr12:122526911-122527291 | Common:3; Rare:125 | ||||
| chr12:122980571-122980969 | Common:2; Rare:114 | ||||
| chr12:123233093-123233486 | Common:2; Rare:128; Clinvar:1 | ||||
| chr12:123364820-123364989 | Common:3; Rare:63 | ||||
| chr12:123584278-123584669 | Common:8; Rare:135 | ||||
| chr12:123601815-123602163 | Common:6; Rare:95 | ||||
| chr12:123633597-123633856 | Common:1; Rare:126; Clinvar:8; Clinvar (benign):1 |