| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67508156-67508467 | Common:1; Rare:61 | ||||
| chr11:68038925-68039062 | Rare:40; Clinvar:1 | ||||
| chr11:68271873-68272102 | Common:2; Rare:97 | ||||
| chr11:68460223-68460360 | Common:2; Rare:59 | ||||
| chr11:68903788-68903958 | Common:5; Rare:79; Clinvar:2; Clinvar (benign):7 | ||||
| chr11:69640983-69641181 | Rare:41 | ||||
| chr11:69675300-69675488 | Rare:54 | ||||
| chr11:70398421-70398591 | Common:2; Rare:61 | ||||
| chr11:71448352-71448590 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71453032-71453258 | Common:1; Rare:64 | ||||
| chr11:71928889-71929058 | Common:1; Rare:58 | ||||
| chr11:72080502-72080762 | Common:1; Rare:54; Clinvar:4 | ||||
| chr11:72793597-72793771 | Rare:41 | ||||
| chr11:73598049-73598287 | Common:3; Rare:62 | ||||
| chr11:73787796-73787930 | Common:1; Rare:29 |