| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120581358-120581569 | Common:1; Rare:75 | ||||
| chr12:120978483-120978783 | Common:1; Rare:103; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:121210035-121210200 | Common:2; Rare:62 | ||||
| chr12:121580241-121580384 | Rare:53 | ||||
| chr12:121672600-121672780 | Common:4; Rare:60 | ||||
| chr12:121802934-121803091 | Rare:38 | ||||
| chr12:121888649-121888859 | Common:2; Rare:66 | ||||
| chr12:122526892-122527262 | Common:3; Rare:121 | ||||
| chr12:122859511-122859826 | Common:1; Rare:103 | ||||
| chr12:122975194-122975241 | Rare:11 | ||||
| chr12:122980571-122980743 | Common:1; Rare:56 | ||||
| chr12:123233096-123233486 | Common:2; Rare:126; Clinvar:1 | ||||
| chr12:123364820-123364983 | Common:3; Rare:61 | ||||
| chr12:123584361-123584744 | Common:7; Rare:137 | ||||
| chr12:123602023-123602156 | Common:3; Rare:47 |