| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45216018-45216140 | Rare:38 | ||||
| chr12:46267370-46267412 | Rare:9 | ||||
| chr12:46372742-46372982 | Rare:98 | ||||
| chr12:47705972-47706088 | Rare:55 | ||||
| chr12:47758836-47759011 | Rare:38 | ||||
| chr12:48105992-48106057 | Rare:15 | ||||
| chr12:48106064-48106123 | Common:1; Rare:18 | ||||
| chr12:48350794-48350950 | Rare:59 | ||||
| chr12:49018736-49018891 | Rare:65 | ||||
| chr12:49131355-49131617 | Common:2; Rare:95 | ||||
| chr12:49186660-49187067 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49188981-49189307 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49568104-49568192 | Common:2; Rare:29 | ||||
| chr12:49828404-49828537 | Rare:45 | ||||
| chr12:50283514-50283656 | Common:1; Rare:43 |