| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:77820815-77821210 | Common:2; Rare:115 | ||||
| chr11:78079579-78079638 | Common:2; Rare:15 | ||||
| chr11:78139526-78139824 | Common:3; Rare:113; Clinvar:3 | ||||
| chr11:78188616-78188969 | Common:3; Rare:110 | ||||
| chr11:83071797-83072131 | Common:4; Rare:93 | ||||
| chr11:83193649-83193778 | Common:1; Rare:54 | ||||
| chr11:83285940-83286087 | Common:3; Rare:62 | ||||
| chr11:85628324-85628610 | Common:7; Rare:90 | ||||
| chr11:85647857-85648088 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:86069065-86069426 | Common:2; Rare:118 | ||||
| chr11:86302189-86302503 | Common:2; Rare:80 | ||||
| chr11:88337660-88337894 | Common:4; Rare:112; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:89178390-89178563 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr11:93741446-93741701 | Common:5; Rare:103 | ||||
| chr11:94493792-94494018 | Common:3; Rare:65; Clinvar (benign):1 |