| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66057946-66059151 | Common:12; Rare:526 | ||||
| chr11:66069882-66071439 | Common:23; Rare:1070; Clinvar:9; Clinvar (benign):6 | ||||
| chr11:66083259-66083659 | Common:1; Rare:76 | ||||
| chr11:66256950-66257400 | Common:4; Rare:124 | ||||
| chr11:66257525-66257845 | Rare:386 | ||||
| chr11:66258094-66258632 | Common:2; Rare:265 | ||||
| chr11:66268294-66268698 | Common:15; Rare:456 | ||||
| chr11:66268618-66269388 | Common:7; Rare:348 | ||||
| chr11:66288451-66288851 | Common:2; Rare:97 | ||||
| chr11:66288835-66288938 | Common:1; Rare:35 | ||||
| chr11:66288972-66289525 | Common:8; Rare:646 | ||||
| chr11:66341271-66342185 | Common:8; Rare:360 | ||||
| chr11:66344391-66344885 | Common:3; Rare:125 | ||||
| chr11:66344938-66345671 | Common:5; Rare:388 | ||||
| chr11:66347280-66348246 | Common:40; Rare:874; Clinvar:3; Clinvar (benign):6 |