| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67482901-67483148 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68038915-68039079 | Rare:51; Clinvar:1 | ||||
| chr11:68049729-68050052 | Rare:103; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr11:68271884-68272108 | Common:2; Rare:95 | ||||
| chr11:68903778-68903938 | Common:4; Rare:77; Clinvar (benign):6 | ||||
| chr11:69640950-69641250 | Common:1; Rare:62 | ||||
| chr11:69641364-69641505 | Rare:36 | ||||
| chr11:69675307-69675487 | Rare:49 | ||||
| chr11:70398420-70398596 | Common:2; Rare:64 | ||||
| chr11:71448352-71448690 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71787350-71787546 | Common:12; Rare:82 | ||||
| chr11:71928572-71928831 | Rare:62 | ||||
| chr11:71928966-71929073 | Common:1; Rare:37 | ||||
| chr11:72009138-72009312 | Rare:69 | ||||
| chr11:72080232-72080336 | Common:6; Rare:15 |