Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61361841-61362021 | Common:1; Rare:43 | ||||
chr11:61362276-61362404 | Common:1; Rare:36; Clinvar:6 | ||||
chr11:61392533-61392654 | Common:2; Rare:42; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429920-61430152 | Common:1; Rare:104; Clinvar:1; Clinvar (benign):3 | ||||
chr11:61792572-61792955 | Common:5; Rare:103 | ||||
chr11:61816138-61816283 | Rare:34 | ||||
chr11:61967313-61967553 | Rare:88; Clinvar:1 | ||||
chr11:61967603-61967806 | Common:1; Rare:81; Clinvar:3 | ||||
chr11:62545614-62545946 | Common:1; Rare:73 | ||||
chr11:62546684-62546936 | Common:1; Rare:79 | ||||
chr11:62601215-62601484 | Common:1; Rare:78 | ||||
chr11:62611546-62611852 | Rare:76 | ||||
chr11:62653273-62653436 | Common:1; Rare:51 | ||||
chr11:62665156-62665418 | Common:5; Rare:122 | ||||
chr11:62679024-62679144 | Rare:39 |