| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53220868-53221277 | Common:2; Rare:97 | ||||
| chr12:53251951-53252237 | Common:3; Rare:109 | ||||
| chr12:53267539-53267848 | Rare:55 | ||||
| chr12:53268050-53268340 | Common:3; Rare:71 | ||||
| chr12:53268418-53268614 | Rare:35 | ||||
| chr12:53295368-53295678 | Common:2; Rare:102 | ||||
| chr12:53299635-53299878 | Common:2; Rare:123 | ||||
| chr12:53299880-53300036 | Rare:67 | ||||
| chr12:53321218-53321675 | Common:2; Rare:152; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr12:53324189-53324317 | Rare:25 | ||||
| chr12:53324443-53324615 | Common:1; Rare:29 | ||||
| chr12:53324863-53325110 | Common:1; Rare:59 | ||||
| chr12:53379816-53380227 | Common:1; Rare:142 | ||||
| chr12:53380354-53380867 | Common:1; Rare:165 | ||||
| chr12:53441173-53441308 | Common:1; Rare:30 |