| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46269095-46269160 | Common:1; Rare:13 | ||||
| chr12:46371283-46371515 | Common:2; Rare:106 | ||||
| chr12:46372696-46372975 | Rare:117 | ||||
| chr12:47079736-47080087 | Common:4; Rare:87 | ||||
| chr12:47705970-47706088 | Rare:55 | ||||
| chr12:47725468-47725707 | Common:1; Rare:40 | ||||
| chr12:47758873-47759011 | Rare:32 | ||||
| chr12:47904986-47905151 | Common:1; Rare:50; Clinvar:1 | ||||
| chr12:48105832-48106196 | Common:2; Rare:114 | ||||
| chr12:48957384-48957569 | Common:2; Rare:53 | ||||
| chr12:49018736-49018943 | Common:1; Rare:87 | ||||
| chr12:49131355-49131592 | Rare:88 | ||||
| chr12:49188488-49188590 | Common:1; Rare:14 | ||||
| chr12:49188981-49189233 | Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264758-49265096 | Common:4; Rare:120 |