| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723847-6724333 | Common:2; Rare:103 | ||||
| chr12:6752908-6753208 | Common:6; Rare:88 | ||||
| chr12:6766092-6766363 | Common:1; Rare:55 | ||||
| chr12:6766420-6766747 | Rare:88 | ||||
| chr12:6829649-6829993 | Common:2; Rare:98 | ||||
| chr12:6851169-6851499 | Rare:73 | ||||
| chr12:6851977-6852243 | Common:1; Rare:70 | ||||
| chr12:6867479-6867675 | Common:2; Rare:105; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6869146-6869293 | Rare:46; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6870071-6870307 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6873246-6873691 | Common:4; Rare:127 | ||||
| chr12:6927575-6927813 | Rare:60 | ||||
| chr12:6943921-6944172 | Common:9; Rare:250; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6967449-6967941 | Rare:160 | ||||
| chr12:6970359-6971135 | Common:10; Rare:247; Clinvar (benign):2 |