Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:67482906-67483154 | Rare:55; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr11:67508091-67508183 | Rare:35 | ||||
chr11:68030381-68030733 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68271900-68272108 | Common:2; Rare:87 | ||||
chr11:68903784-68903949 | Common:4; Rare:81; Clinvar (benign):6 | ||||
chr11:69675309-69675488 | Rare:50 | ||||
chr11:70398320-70398596 | Common:2; Rare:97 | ||||
chr11:70826702-70826840 | Rare:31 | ||||
chr11:71448338-71448711 | Common:4; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
chr11:71928923-71929058 | Common:1; Rare:45 | ||||
chr11:72041056-72041331 | Common:1; Rare:50 | ||||
chr11:72041848-72041880 | Rare:8 | ||||
chr11:72080449-72080845 | Common:2; Rare:89; Clinvar:7 | ||||
chr11:72103226-72103531 | Rare:87 | ||||
chr11:72112658-72113033 | Common:5; Rare:144 |