| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6869220-6869293 | Rare:21 | ||||
| chr12:6870050-6870309 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6873245-6873483 | Common:2; Rare:69 | ||||
| chr12:6927557-6927818 | Rare:65 | ||||
| chr12:6928169-6928382 | Common:2; Rare:47 | ||||
| chr12:6943926-6944173 | Common:8; Rare:247; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946471-6946722 | Common:2; Rare:73 | ||||
| chr12:6967603-6967716 | Rare:35 | ||||
| chr12:6970411-6971078 | Common:9; Rare:211; Clinvar (benign):2 | ||||
| chr12:7108442-7108727 | Common:1; Rare:79 | ||||
| chr12:7109186-7109409 | Rare:59 | ||||
| chr12:7130240-7130440 | Common:5; Rare:54 | ||||
| chr12:8032617-8032786 | Rare:60 | ||||
| chr12:8662539-8662569 | Rare:5 | ||||
| chr12:8662613-8662963 | Common:4; Rare:72 |