| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61769571-61769948 | Common:3; Rare:70 | ||||
| chr11:61923309-61923558 | Common:2; Rare:46 | ||||
| chr11:61923684-61923894 | Common:1; Rare:41 | ||||
| chr11:61955803-61955979 | Rare:61; Clinvar:3; Clinvar (pathogenic):4 | ||||
| chr11:61959134-61959268 | Common:1; Rare:22 | ||||
| chr11:61963888-61964186 | Common:4; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:61968221-61968308 | Rare:29 | ||||
| chr11:61968409-61968529 | Rare:32 | ||||
| chr11:61971879-61972096 | Common:1; Rare:44 | ||||
| chr11:61973103-61973207 | Rare:13 | ||||
| chr11:62042061-62042184 | Common:1; Rare:10 | ||||
| chr11:62054545-62054831 | Common:2; Rare:37 | ||||
| chr11:62112579-62112698 | Common:3; Rare:40 | ||||
| chr11:62338128-62338166 | Rare:14 | ||||
| chr11:62382282-62382359 | Rare:11 |