| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124673712-124673935 | Common:4; Rare:66 | ||||
| chr11:125592524-125592930 | Common:6; Rare:133 | ||||
| chr11:126211641-126211807 | Rare:76 | ||||
| chr11:126268556-126268619 | Common:2; Rare:16 | ||||
| chr11:126268787-126269207 | Common:2; Rare:161; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126355553-126355787 | Rare:62 | ||||
| chr11:134253319-134253602 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:991109-991251 | Common:1; Rare:53 | ||||
| chr12:4648989-4649126 | Common:1; Rare:39 | ||||
| chr12:6452031-6452180 | Common:1; Rare:30 | ||||
| chr12:6493240-6493389 | Common:5; Rare:41 | ||||
| chr12:6723858-6724165 | Common:1; Rare:64 | ||||
| chr12:6752949-6753002 | Rare:13 | ||||
| chr12:6873282-6873483 | Common:2; Rare:57 | ||||
| chr12:6970591-6970964 | Common:4; Rare:112; Clinvar (benign):1 |