| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46549863-46550091 | Common:1; Rare:43 | ||||
| chr12:47080560-47080963 | Common:1; Rare:97 | ||||
| chr12:48135204-48135602 | Common:1; Rare:88; Clinvar (benign):2 | ||||
| chr12:48667662-48667693 | Rare:13 | ||||
| chr12:48784781-48784834 | Rare:9 | ||||
| chr12:48787203-48787454 | Rare:46 | ||||
| chr12:48787966-48788012 | Rare:3 | ||||
| chr12:48930833-48931152 | Rare:54 | ||||
| chr12:49635125-49635370 | Rare:74 | ||||
| chr12:49764876-49765091 | Common:2; Rare:57 | ||||
| chr12:50089963-50090207 | Common:1; Rare:45 | ||||
| chr12:50149283-50149335 | Rare:8 | ||||
| chr12:50203388-50203475 | Rare:22 | ||||
| chr12:50221326-50221460 | Rare:23 | ||||
| chr12:51077910-51077996 | Rare:16 |