Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:30586096-30586315 | Common:1; Rare:82 | ||||
chr11:31369724-31369882 | Rare:48 | ||||
chr11:31509575-31509790 | Common:1; Rare:67 | ||||
chr11:31811306-31811469 | Rare:21 | ||||
chr11:32583663-32583929 | Rare:95 | ||||
chr11:33161443-33161678 | Common:6; Rare:65 | ||||
chr11:33257133-33257427 | Common:3; Rare:94 | ||||
chr11:33736410-33736586 | Common:1; Rare:61 | ||||
chr11:33774493-33774650 | Common:2; Rare:55 | ||||
chr11:34052138-34052531 | Common:4; Rare:178 | ||||
chr11:34053323-34053455 | Rare:33 | ||||
chr11:34105471-34105660 | Common:2; Rare:62 | ||||
chr11:34438776-34438997 | Common:2; Rare:73; Clinvar (benign):1 | ||||
chr11:34916287-34916676 | Common:10; Rare:158; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr11:35138954-35139174 | Common:1; Rare:52 |