| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:615946-616027 | Rare:24 | ||||
| chr11:695737-695821 | Rare:30 | ||||
| chr11:777465-777611 | Common:1; Rare:64 | ||||
| chr11:809498-809622 | Common:2; Rare:36 | ||||
| chr11:809808-810037 | Common:2; Rare:104 | ||||
| chr11:842490-842978 | Common:8; Rare:200 | ||||
| chr11:843937-844159 | Common:1; Rare:57 | ||||
| chr11:1309547-1309856 | Common:3; Rare:129 | ||||
| chr11:1838747-1839046 | Common:1; Rare:80; Clinvar:1 | ||||
| chr11:1871206-1871357 | Common:3; Rare:52 | ||||
| chr11:1919444-1919781 | Rare:86; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:1925095-1925276 | Rare:63 | ||||
| chr11:1933718-1934008 | Rare:96; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:3641989-3642164 | Common:6; Rare:60 | ||||
| chr11:3797474-3797855 | Rare:137 |