| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69640972-69641181 | Rare:42 | ||||
| chr11:69675300-69675503 | Rare:57 | ||||
| chr11:70398417-70398596 | Common:2; Rare:65 | ||||
| chr11:70661782-70661909 | Rare:33 | ||||
| chr11:70662191-70662409 | Common:1; Rare:64 | ||||
| chr11:70826683-70826840 | Rare:32 | ||||
| chr11:70827126-70827316 | Common:1; Rare:31 | ||||
| chr11:71448288-71448750 | Common:5; Rare:122; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452985-71453249 | Common:3; Rare:72 | ||||
| chr11:71787350-71787537 | Common:11; Rare:75 | ||||
| chr11:71928887-71929098 | Common:1; Rare:69 | ||||
| chr11:72041056-72041308 | Common:1; Rare:45 | ||||
| chr11:72041521-72041722 | Rare:32 | ||||
| chr11:72041846-72042012 | Common:2; Rare:33 | ||||
| chr11:72080432-72080884 | Common:2; Rare:107; Clinvar:9 |