| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120249551-120249771 | Common:1; Rare:36 | ||||
| chr12:120437842-120438229 | Common:2; Rare:143; Clinvar (benign):2 | ||||
| chr12:120446353-120446483 | Common:1; Rare:60 | ||||
| chr12:120469596-120469889 | Common:3; Rare:103 | ||||
| chr12:120495852-120496228 | Common:7; Rare:126 | ||||
| chr12:120534308-120534377 | Rare:26 | ||||
| chr12:120581331-120581548 | Common:1; Rare:80 | ||||
| chr12:120978279-120978840 | Common:3; Rare:153; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr12:121038972-121039308 | Common:3; Rare:69 | ||||
| chr12:121210007-121210152 | Common:3; Rare:50 | ||||
| chr12:121296702-121296879 | Common:1; Rare:55 | ||||
| chr12:121399907-121400170 | Common:3; Rare:101 | ||||
| chr12:121712651-121712844 | Common:3; Rare:72 | ||||
| chr12:121802931-121803109 | Common:1; Rare:45 | ||||
| chr12:121803141-121803318 | Rare:50 |