Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:67428336-67428537 | Rare:69 | ||||
chr11:67443458-67443590 | Common:1; Rare:45 | ||||
chr11:68030412-68030733 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68038915-68039053 | Rare:41; Clinvar:1 | ||||
chr11:68271889-68272102 | Common:2; Rare:93 | ||||
chr11:68903800-68903938 | Common:4; Rare:61; Clinvar (benign):6 | ||||
chr11:69675309-69675519 | Rare:56 | ||||
chr11:70398421-70398596 | Common:2; Rare:63 | ||||
chr11:71448321-71448720 | Common:5; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
chr11:72041056-72041295 | Common:1; Rare:42 | ||||
chr11:72080471-72080812 | Common:1; Rare:75; Clinvar:5 | ||||
chr11:72103207-72103518 | Rare:90 | ||||
chr11:72722288-72722417 | Rare:24 | ||||
chr11:72781662-72781958 | Common:1; Rare:87 | ||||
chr11:73598061-73598281 | Common:2; Rare:58 |