| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33736391-33736581 | Common:2; Rare:62 | ||||
| chr11:33774493-33774646 | Common:2; Rare:53 | ||||
| chr11:34105517-34105697 | Common:2; Rare:64 | ||||
| chr11:34438808-34438997 | Common:2; Rare:62; Clinvar (benign):1 | ||||
| chr11:34916282-34916676 | Common:10; Rare:160; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138954-35139207 | Common:1; Rare:56 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43680439-43680755 | Common:2; Rare:74 | ||||
| chr11:43880680-43880945 | Common:2; Rare:73 | ||||
| chr11:45917824-45918180 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46700555-46700796 | Common:1; Rare:65 | ||||
| chr11:46846207-46846414 | Common:1; Rare:59 | ||||
| chr11:47214814-47215123 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248791-47248925 | Rare:54 | ||||
| chr11:47269545-47269690 | Common:1; Rare:50 |