| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50103730-50104130 | Rare:127 | ||||
| chr12:50111618-50112283 | Common:7; Rare:405 | ||||
| chr12:50112204-50112618 | Rare:189; Clinvar (benign):2 | ||||
| chr12:50112550-50112900 | Common:4; Rare:143 | ||||
| chr12:50166630-50167851 | Common:22; Rare:907 | ||||
| chr12:50220346-50220746 | Common:2; Rare:75 | ||||
| chr12:50221317-50222495 | Common:1; Rare:673 | ||||
| chr12:50222540-50223202 | Common:2; Rare:216 | ||||
| chr12:50283254-50283812 | Common:21; Rare:536 | ||||
| chr12:50283936-50284562 | Common:2; Rare:99 | ||||
| chr12:50351127-50351527 | Common:3; Rare:182 | ||||
| chr12:50400627-50402157 | Common:11; Rare:1129 | ||||
| chr12:50504729-50505224 | Common:13; Rare:425 | ||||
| chr12:50505444-50505844 | Common:3; Rare:99 | ||||
| chr12:50763410-50763720 | Common:10; Rare:84 |