Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73167985-73168119 | Rare:29 | ||||
chr10:100987454-100987535 | Rare:40 | ||||
chr10:101588045-101588326 | Rare:111 | ||||
chr10:125823247-125823550 | Rare:87 | ||||
chr11:1309621-1309778 | Common:1; Rare:73 | ||||
chr11:2138314-2138488 | Common:1; Rare:50 | ||||
chr11:6481310-6481527 | Common:4; Rare:89 | ||||
chr11:47578959-47579081 | Rare:63; Clinvar:2 | ||||
chr11:61333096-61333251 | Rare:50 | ||||
chr11:61429946-61430136 | Common:1; Rare:81; Clinvar (benign):1 | ||||
chr11:61792562-61792895 | Common:5; Rare:90 | ||||
chr11:62665171-62665308 | Common:3; Rare:51 | ||||
chr11:68903807-68903915 | Common:3; Rare:45; Clinvar (benign):2 | ||||
chr11:73876811-73877010 | Common:3; Rare:47 | ||||
chr11:74949090-74949283 | Common:5; Rare:47 |