| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53097773-53097880 | Rare:32 | ||||
| chr12:53180411-53180792 | Common:3; Rare:211 | ||||
| chr12:53180830-53181180 | Common:10; Rare:181 | ||||
| chr12:53220157-53220481 | Common:2; Rare:95 | ||||
| chr12:53220835-53221235 | Common:5; Rare:171 | ||||
| chr12:53231870-53232100 | Rare:86 | ||||
| chr12:53232150-53232497 | Common:5; Rare:138 | ||||
| chr12:53251983-53252248 | Common:6; Rare:185 | ||||
| chr12:53268103-53268340 | Common:4; Rare:107 | ||||
| chr12:53295413-53295630 | Common:2; Rare:140 | ||||
| chr12:53299421-53299802 | Common:4; Rare:143 | ||||
| chr12:53321175-53321446 | Common:2; Rare:88; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:53321518-53321715 | Common:2; Rare:83; Clinvar:4 | ||||
| chr12:53324830-53325055 | Common:2; Rare:114 | ||||
| chr12:53344608-53344914 | Common:1; Rare:58 |