| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66851127-66851425 | Rare:73; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:66871140-66871363 | Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:67066534-67066769 | Common:1; Rare:44 | ||||
| chr11:67441149-67441354 | Rare:77 | ||||
| chr11:68041247-68041283 | Rare:14; Clinvar:1 | ||||
| chr11:69470458-69470578 | Common:1; Rare:22 | ||||
| chr11:69985670-69985962 | Common:2; Rare:79 | ||||
| chr11:72754521-72754738 | Common:1; Rare:48 | ||||
| chr11:75156124-75156386 | Common:2; Rare:38 | ||||
| chr11:75163129-75163260 | Rare:27 | ||||
| chr11:76770268-76770392 | Rare:18 | ||||
| chr11:78171018-78171251 | Rare:49 | ||||
| chr11:78314673-78314829 | Rare:27 | ||||
| chr11:86955987-86956157 | Common:2; Rare:55 | ||||
| chr11:93733584-93733686 | Rare:39 |