| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66480212-66480450 | Common:3; Rare:63 | ||||
| chr11:66510551-66510702 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66592997-66593259 | Common:1; Rare:96 | ||||
| chr11:66616379-66616703 | Common:2; Rare:103 | ||||
| chr11:66616841-66617388 | Common:1; Rare:156 | ||||
| chr11:66638417-66638763 | Common:4; Rare:144 | ||||
| chr11:66677765-66678018 | Common:1; Rare:102 | ||||
| chr11:66688810-66689040 | Common:4; Rare:46 | ||||
| chr11:66721215-66721443 | Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:66744623-66744887 | Common:3; Rare:109 | ||||
| chr11:66856197-66856426 | Common:1; Rare:76 | ||||
| chr11:66958344-66958612 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67006665-67006815 | Common:2; Rare:40 | ||||
| chr11:67056792-67056887 | Rare:29 | ||||
| chr11:67240021-67240156 | Rare:25 |