Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61311790-61312013 | Rare:71 | ||||
chr11:61332981-61333323 | Common:1; Rare:121 | ||||
chr11:61361837-61362051 | Common:2; Rare:52; Clinvar:2 | ||||
chr11:61362196-61362433 | Common:2; Rare:69; Clinvar:8; Clinvar (benign):1 | ||||
chr11:61392371-61392441 | Rare:8; Clinvar:1 | ||||
chr11:61392527-61392678 | Common:2; Rare:50; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr11:61429182-61429490 | Common:3; Rare:98 | ||||
chr11:61429835-61430176 | Common:1; Rare:143; Clinvar:3; Clinvar (benign):6 | ||||
chr11:61508523-61508750 | Rare:58 | ||||
chr11:61792549-61792759 | Common:5; Rare:75 | ||||
chr11:61792824-61793031 | Rare:46 | ||||
chr11:61810853-61811022 | Rare:29 | ||||
chr11:61816084-61816539 | Rare:132 | ||||
chr11:61816545-61816582 | Rare:4 | ||||
chr11:61816735-61817209 | Common:1; Rare:109 |