| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:71448332-71448632 | Common:3; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928568-71928715 | Rare:38 | ||||
| chr11:71928889-71929067 | Common:1; Rare:60 | ||||
| chr11:73760628-73760750 | Common:2; Rare:31 | ||||
| chr11:73876794-73877030 | Common:4; Rare:64 | ||||
| chr11:74949062-74949310 | Common:6; Rare:71 | ||||
| chr11:77820867-77821207 | Common:1; Rare:100 | ||||
| chr11:78188597-78188939 | Common:2; Rare:107 | ||||
| chr11:83071825-83072106 | Common:4; Rare:78 | ||||
| chr11:83193658-83193786 | Common:1; Rare:55 | ||||
| chr11:83285922-83286055 | Common:3; Rare:62 | ||||
| chr11:85628332-85628633 | Common:7; Rare:100 | ||||
| chr11:86302070-86302474 | Common:3; Rare:86 | ||||
| chr11:86672138-86672237 | Rare:19 | ||||
| chr11:86955344-86955654 | Common:1; Rare:101; Clinvar (benign):1 |