| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52249092-52249357 | Rare:135 | ||||
| chr12:52291226-52291626 | Common:9; Rare:207; Clinvar:1 | ||||
| chr12:52903179-52904117 | Common:26; Rare:379 | ||||
| chr12:52904751-52905412 | Common:13; Rare:292; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:52906145-52906645 | Common:4; Rare:249 | ||||
| chr12:52906572-52906793 | Rare:76 | ||||
| chr12:52906970-52907526 | Common:13; Rare:196 | ||||
| chr12:52926029-52926491 | Common:3; Rare:161 | ||||
| chr12:52926480-52927150 | Common:3; Rare:171 | ||||
| chr12:52948792-52949236 | Common:6; Rare:301; Clinvar:3 | ||||
| chr12:52949705-52950091 | Common:1; Rare:152 | ||||
| chr12:52951473-52952205 | Rare:336; Clinvar:14 | ||||
| chr12:53005969-53006684 | Common:13; Rare:599 | ||||
| chr12:53006790-53007170 | Common:5; Rare:214 | ||||
| chr12:53046855-53047328 | Common:10; Rare:262 |