| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119593618-119593789 | Rare:32 | ||||
| chr12:119667934-119668038 | Rare:25 | ||||
| chr12:119668101-119668203 | Common:1; Rare:21 | ||||
| chr12:119877267-119877532 | Common:2; Rare:59 | ||||
| chr12:120116655-120116935 | Common:5; Rare:82 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437881-120438241 | Common:2; Rare:137; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446353-120446485 | Common:1; Rare:62 | ||||
| chr12:120469580-120469890 | Common:3; Rare:110 | ||||
| chr12:120495845-120496221 | Common:7; Rare:127 | ||||
| chr12:120581353-120581539 | Common:1; Rare:69 | ||||
| chr12:120978278-120978771 | Common:2; Rare:138; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:121210056-121210152 | Common:2; Rare:33 | ||||
| chr12:121352336-121352648 | Common:3; Rare:118 | ||||
| chr12:121399916-121400189 | Common:3; Rare:103 |