| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120116610-120116961 | Common:6; Rare:106 | ||||
| chr12:120117024-120117291 | Common:3; Rare:68 | ||||
| chr12:120194683-120194832 | Common:1; Rare:56 | ||||
| chr12:120197223-120197477 | Rare:68 | ||||
| chr12:120201074-120201392 | Common:2; Rare:99 | ||||
| chr12:120224721-120224824 | Common:1; Rare:33 | ||||
| chr12:120437842-120438270 | Common:3; Rare:158; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446224-120446504 | Common:2; Rare:105 | ||||
| chr12:120469421-120469498 | Common:1; Rare:16 | ||||
| chr12:120469542-120469906 | Common:3; Rare:127 | ||||
| chr12:120495843-120496246 | Common:8; Rare:134 | ||||
| chr12:120529086-120529252 | Common:2; Rare:63 | ||||
| chr12:120581330-120581588 | Common:1; Rare:89 | ||||
| chr12:120686345-120686569 | Common:2; Rare:64 | ||||
| chr12:120686949-120687155 | Common:1; Rare:72 |