| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31589620-31590040 | Common:2; Rare:150 | ||||
| chr12:31590290-31590758 | Common:6; Rare:245 | ||||
| chr12:31590876-31591271 | Common:1; Rare:247 | ||||
| chr12:31658950-31659680 | Common:5; Rare:291 | ||||
| chr12:31728989-31729339 | Common:2; Rare:192 | ||||
| chr12:31959262-31959608 | Common:5; Rare:166 | ||||
| chr12:32106588-32106959 | Common:6; Rare:139 | ||||
| chr12:32399160-32399604 | Common:9; Rare:189 | ||||
| chr12:32399695-32399998 | Common:3; Rare:154 | ||||
| chr12:32679050-32679342 | Common:2; Rare:177; Clinvar (benign):4 | ||||
| chr12:32754950-32755420 | Common:2; Rare:223; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr12:32755848-32756021 | Rare:107 | ||||
| chr12:32896735-32896876 | Common:3; Rare:88; Clinvar:8; Clinvar (benign):9 | ||||
| chr12:32896921-32897365 | Common:5; Rare:220 | ||||
| chr12:38316664-38316891 | Common:3; Rare:59 |