| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49131301-49131621 | Common:2; Rare:126 | ||||
| chr12:49188482-49188593 | Common:1; Rare:16 | ||||
| chr12:49188949-49189296 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49227948-49228028 | Rare:10 | ||||
| chr12:49264781-49265083 | Common:4; Rare:105 | ||||
| chr12:49367179-49367541 | Common:1; Rare:103 | ||||
| chr12:49568104-49568211 | Common:2; Rare:36 | ||||
| chr12:49741291-49741578 | Rare:80 | ||||
| chr12:49828392-49828554 | Common:1; Rare:55 | ||||
| chr12:49843092-49843138 | Rare:14 | ||||
| chr12:50025416-50025741 | Common:2; Rare:86 | ||||
| chr12:50085258-50085399 | Common:1; Rare:40 | ||||
| chr12:50103881-50104009 | Rare:28 | ||||
| chr12:50167269-50167533 | Common:2; Rare:82 | ||||
| chr12:50283500-50283656 | Common:1; Rare:48 |