| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52451441-52451661 | Common:2; Rare:80; Clinvar (pathogenic):1 | ||||
| chr12:52451931-52452193 | Common:3; Rare:97 | ||||
| chr12:52452265-52452419 | Common:2; Rare:31 | ||||
| chr12:52471167-52471445 | Common:1; Rare:118 | ||||
| chr12:52490699-52491172 | Common:4; Rare:166 | ||||
| chr12:52491701-52492132 | Common:3; Rare:100 | ||||
| chr12:52492372-52492460 | Rare:16 | ||||
| chr12:52492492-52492757 | Common:7; Rare:88; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr12:52493081-52493199 | Common:1; Rare:44 | ||||
| chr12:52493206-52493613 | Rare:82 | ||||
| chr12:52517567-52518504 | Common:1; Rare:245; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:52518509-52519041 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:52519147-52519284 | Common:2; Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:52520515-52520576 | Rare:8 | ||||
| chr12:52679757-52680117 | Common:1; Rare:119; Clinvar:5 |