| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8868230-8868624 | Common:4; Rare:129; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:9115839-9116283 | Common:3; Rare:90 | ||||
| chr12:9760882-9760904 | Common:1; Rare:5 | ||||
| chr12:9869336-9869457 | Common:1; Rare:20 | ||||
| chr12:10098922-10099037 | Rare:27 | ||||
| chr12:10390033-10390142 | Rare:22 | ||||
| chr12:10613524-10613645 | Rare:51 | ||||
| chr12:11171163-11171243 | Rare:34 | ||||
| chr12:11171553-11171633 | Common:1; Rare:27 | ||||
| chr12:12356999-12357207 | Common:4; Rare:107 | ||||
| chr12:12717211-12717470 | Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725661-12725929 | Common:2; Rare:58 | ||||
| chr12:12785440-12785666 | Common:2; Rare:53 | ||||
| chr12:12891314-12891575 | Common:1; Rare:50 | ||||
| chr12:13000204-13000468 | Common:2; Rare:89 |