| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53180825-53181176 | Common:6; Rare:96 | ||||
| chr12:53200601-53200953 | Common:5; Rare:73 | ||||
| chr12:53207127-53207406 | Common:1; Rare:47 | ||||
| chr12:53220310-53220499 | Common:2; Rare:34 | ||||
| chr12:53220864-53221292 | Common:3; Rare:101 | ||||
| chr12:53251951-53252381 | Common:3; Rare:131 | ||||
| chr12:53267722-53267834 | Rare:19 | ||||
| chr12:53268080-53268340 | Common:3; Rare:66 | ||||
| chr12:53268359-53268574 | Common:1; Rare:36 | ||||
| chr12:53295383-53295642 | Common:2; Rare:87 | ||||
| chr12:53299588-53299834 | Common:3; Rare:137 | ||||
| chr12:53321241-53321632 | Common:2; Rare:142; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr12:53321661-53321723 | Rare:12 | ||||
| chr12:53324215-53324607 | Common:1; Rare:63 | ||||
| chr12:53324877-53325134 | Common:1; Rare:61 |