Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:66677864-66677971 | Rare:39 | ||||
chr11:67508078-67508143 | Rare:19 | ||||
chr11:67508149-67508433 | Common:1; Rare:56 | ||||
chr11:68030412-68030730 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68271895-68272123 | Common:2; Rare:95 | ||||
chr11:68903774-68903955 | Common:5; Rare:86; Clinvar:1; Clinvar (benign):7 | ||||
chr11:70398431-70398601 | Common:2; Rare:62 | ||||
chr11:71448360-71448590 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
chr11:72041857-72042077 | Common:1; Rare:49 | ||||
chr11:72080502-72080853 | Common:1; Rare:78; Clinvar:5 | ||||
chr11:72112264-72112520 | Rare:65 | ||||
chr11:72752396-72752572 | Common:2; Rare:53 | ||||
chr11:73598055-73598281 | Common:3; Rare:59 | ||||
chr11:73760679-73760884 | Common:2; Rare:43 | ||||
chr11:73761010-73761335 | Common:3; Rare:98 |