| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95942883-95943076 | Common:2; Rare:39 | ||||
| chr12:96035361-96035435 | Rare:21 | ||||
| chr12:96035514-96035795 | Common:2; Rare:64 | ||||
| chr12:96399585-96399799 | Rare:54 | ||||
| chr12:96400211-96400709 | Common:2; Rare:182 | ||||
| chr12:96907081-96907495 | Common:3; Rare:134 | ||||
| chr12:96907956-96908099 | Common:1; Rare:22 | ||||
| chr12:98515059-98515817 | Common:5; Rare:231; Clinvar:5 | ||||
| chr12:98515972-98516078 | Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:98516134-98516327 | Rare:67 | ||||
| chr12:98516383-98516499 | Common:1; Rare:41 | ||||
| chr12:98516508-98516578 | Common:1; Rare:21 | ||||
| chr12:98593382-98593792 | Common:2; Rare:140; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644703-98644909 | Common:3; Rare:62 | ||||
| chr12:98644935-98645320 | Common:2; Rare:111 |