| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:59668983-59669328 | Rare:119 | ||||
| chr11:59755265-59755465 | Common:2; Rare:65 | ||||
| chr11:59810604-59810858 | Common:3; Rare:99 | ||||
| chr11:60841912-60842120 | Common:2; Rare:77 | ||||
| chr11:60906513-60906808 | Rare:73 | ||||
| chr11:60913823-60914210 | Common:1; Rare:77 | ||||
| chr11:60952336-60952462 | Rare:26 | ||||
| chr11:61161417-61161759 | Common:1; Rare:97 | ||||
| chr11:61333034-61333266 | Rare:81 | ||||
| chr11:61361843-61361973 | Common:1; Rare:32 | ||||
| chr11:61362243-61362404 | Common:2; Rare:47; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392526-61392652 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429912-61430164 | Common:1; Rare:115; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792555-61792944 | Common:6; Rare:109 | ||||
| chr11:61827871-61828198 | Common:1; Rare:55 |