| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31073743-31073910 | Common:8; Rare:63 | ||||
| chr12:31074079-31074266 | Common:1; Rare:38 | ||||
| chr12:31324104-31324312 | Rare:43 | ||||
| chr12:31326083-31326433 | Common:4; Rare:115 | ||||
| chr12:31729010-31729312 | Common:1; Rare:94 | ||||
| chr12:31959276-31959482 | Common:2; Rare:65 | ||||
| chr12:32679086-32679358 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755242-32755366 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:32755477-32755629 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:32755853-32756017 | Rare:61 | ||||
| chr12:32896796-32896990 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:38905540-38905813 | Common:6; Rare:78 | ||||
| chr12:42326008-42326206 | Common:1; Rare:63 | ||||
| chr12:43758745-43759007 | Common:2; Rare:73; Clinvar:2 | ||||
| chr12:43806219-43806393 | Common:2; Rare:56 |