| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188981-49189282 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264742-49265096 | Common:5; Rare:124 | ||||
| chr12:49367179-49367534 | Common:1; Rare:100 | ||||
| chr12:49568104-49568216 | Common:2; Rare:37 | ||||
| chr12:49623262-49623561 | Common:1; Rare:86 | ||||
| chr12:49828391-49828594 | Common:1; Rare:73 | ||||
| chr12:50085307-50085380 | Common:1; Rare:16 | ||||
| chr12:50283452-50283672 | Common:3; Rare:68 | ||||
| chr12:50400789-50400997 | Common:1; Rare:70 | ||||
| chr12:50763925-50764137 | Common:1; Rare:58 | ||||
| chr12:50924476-50924752 | Common:3; Rare:81 | ||||
| chr12:51026319-51026495 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048084-51048359 | Common:2; Rare:92 | ||||
| chr12:51173061-51173185 | Rare:24 | ||||
| chr12:51270278-51270312 | Rare:9 |