| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68030390-68030744 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039083 | Rare:51; Clinvar:1 | ||||
| chr11:68213507-68213639 | Rare:77 | ||||
| chr11:68460560-68460817 | Common:3; Rare:88 | ||||
| chr11:68903774-68903915 | Common:3; Rare:66; Clinvar (benign):2 | ||||
| chr11:71452953-71453280 | Common:4; Rare:90 | ||||
| chr11:71998850-71999001 | Rare:33 | ||||
| chr11:72070054-72070185 | Rare:16 | ||||
| chr11:72223763-72223932 | Rare:48 | ||||
| chr11:72228853-72229175 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
| chr11:72722077-72722134 | Rare:9 | ||||
| chr11:72752374-72752554 | Common:3; Rare:52 | ||||
| chr11:72814271-72814436 | Common:1; Rare:51 | ||||
| chr11:73218108-73218371 | Common:1; Rare:49 | ||||
| chr11:73272139-73272366 | Common:2; Rare:46 |