Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65860404-65860779 | Common:2; Rare:122 | ||||
chr11:65919054-65919280 | Rare:81 | ||||
chr11:66002105-66002266 | Rare:48; Clinvar:4 | ||||
chr11:66002465-66002516 | Rare:11 | ||||
chr11:66289069-66289417 | Common:1; Rare:88 | ||||
chr11:66347586-66347896 | Common:5; Rare:73 | ||||
chr11:66480239-66480450 | Common:1; Rare:56 | ||||
chr11:66593061-66593223 | Common:1; Rare:57 | ||||
chr11:66843334-66843456 | Common:5; Rare:62 | ||||
chr11:67056789-67056905 | Rare:36 | ||||
chr11:67428349-67428533 | Rare:66 | ||||
chr11:67482947-67483153 | Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
chr11:67508048-67508416 | Common:1; Rare:85 | ||||
chr11:67508638-67508759 | Common:2; Rare:43 | ||||
chr11:68030404-68030744 | Common:3; Rare:91; Clinvar:1; Clinvar (benign):2 |