| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:43806220-43806385 | Common:2; Rare:54 | ||||
| chr12:45216007-45216184 | Rare:54 | ||||
| chr12:45990543-45990922 | Common:2; Rare:121 | ||||
| chr12:46268593-46268655 | Rare:14 | ||||
| chr12:46371341-46371516 | Common:2; Rare:77 | ||||
| chr12:47079523-47079621 | Common:1; Rare:21 | ||||
| chr12:47705970-47706119 | Rare:64 | ||||
| chr12:47758870-47759011 | Rare:32 | ||||
| chr12:48105994-48106110 | Rare:31 | ||||
| chr12:48350777-48350889 | Rare:34 | ||||
| chr12:49018741-49018926 | Rare:74 | ||||
| chr12:49131355-49131592 | Rare:88 | ||||
| chr12:49188981-49189281 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264792-49265082 | Common:4; Rare:97 | ||||
| chr12:49568104-49568190 | Common:2; Rare:28 |