| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46372651-46372965 | Rare:131 | ||||
| chr12:47079504-47079647 | Common:1; Rare:27 | ||||
| chr12:47705955-47706093 | Rare:61 | ||||
| chr12:47758840-47759027 | Common:1; Rare:39 | ||||
| chr12:47904979-47905113 | Common:1; Rare:39; Clinvar:1 | ||||
| chr12:48105972-48106117 | Common:1; Rare:40 | ||||
| chr12:48350863-48351082 | Common:5; Rare:80 | ||||
| chr12:48815457-48815624 | Common:1; Rare:37 | ||||
| chr12:49018737-49018984 | Common:1; Rare:102; Clinvar (benign):1 | ||||
| chr12:49131325-49131606 | Common:2; Rare:114 | ||||
| chr12:49264752-49265127 | Common:5; Rare:135 | ||||
| chr12:49568074-49568218 | Common:2; Rare:51 | ||||
| chr12:49828380-49828592 | Common:1; Rare:80 | ||||
| chr12:50025380-50025788 | Common:2; Rare:112 | ||||
| chr12:50283477-50283662 | Common:2; Rare:58 |