| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:36510229-36510374 | Rare:44 | ||||
| chr11:43358844-43359050 | Rare:88 | ||||
| chr11:44066183-44066530 | Common:3; Rare:90 | ||||
| chr11:45804974-45805156 | Common:2; Rare:41; Clinvar:3 | ||||
| chr11:45847184-45847521 | Common:2; Rare:141 | ||||
| chr11:45917824-45918180 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46120934-46121037 | Rare:9 | ||||
| chr11:46121068-46121323 | Common:2; Rare:42 | ||||
| chr11:46593971-46594133 | Common:2; Rare:42 | ||||
| chr11:46617196-46617585 | Common:5; Rare:109 | ||||
| chr11:46700551-46700830 | Common:1; Rare:72 | ||||
| chr11:46846218-46846412 | Common:1; Rare:53 | ||||
| chr11:47176837-47177069 | Rare:98 | ||||
| chr11:47214357-47214509 | Common:1; Rare:12 | ||||
| chr11:47214840-47215110 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 |