Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65857005-65857310 | Common:4; Rare:93 | ||||
chr11:65860174-65860557 | Common:3; Rare:125 | ||||
chr11:65860601-65860765 | Rare:60 | ||||
chr11:65861261-65861385 | Common:1; Rare:39 | ||||
chr11:65918984-65919280 | Common:2; Rare:118 | ||||
chr11:65976519-65976635 | Rare:36 | ||||
chr11:66002094-66002796 | Common:4; Rare:196; Clinvar:7; Clinvar (benign):3 | ||||
chr11:66347584-66347879 | Common:5; Rare:68 | ||||
chr11:66480236-66480446 | Common:1; Rare:56 | ||||
chr11:66593096-66593232 | Common:1; Rare:48 | ||||
chr11:66616426-66616631 | Common:1; Rare:53 | ||||
chr11:66843334-66843456 | Common:5; Rare:62 | ||||
chr11:67428349-67428532 | Rare:66 | ||||
chr11:68030381-68030757 | Common:3; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68271930-68272102 | Common:2; Rare:78 |