Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:414962-415188 | Common:1; Rare:45 | ||||
chr11:504828-505141 | Common:4; Rare:76 | ||||
chr11:506705-507001 | Common:3; Rare:97 | ||||
chr11:560707-561016 | Common:6; Rare:143 | ||||
chr11:576412-576528 | Rare:47 | ||||
chr11:615919-616256 | Common:1; Rare:100 | ||||
chr11:695753-695821 | Rare:26 | ||||
chr11:747404-747536 | Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
chr11:777459-777627 | Common:1; Rare:74 | ||||
chr11:809119-809347 | Common:5; Rare:58 | ||||
chr11:809786-810037 | Common:2; Rare:114 | ||||
chr11:812541-812736 | Common:1; Rare:76 | ||||
chr11:842497-842918 | Common:7; Rare:176 | ||||
chr11:1309555-1309879 | Common:3; Rare:129 | ||||
chr11:1852867-1853192 | Common:5; Rare:83 |