Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65416325-65416644 | Common:2; Rare:90 | ||||
chr11:65422623-65422804 | Common:2; Rare:52 | ||||
chr11:65487612-65488079 | Common:1; Rare:88 | ||||
chr11:65496170-65496418 | Common:2; Rare:46 | ||||
chr11:65497395-65497869 | Common:1; Rare:212 | ||||
chr11:65498558-65498671 | Rare:70 | ||||
chr11:65504257-65505190 | Common:3; Rare:444 | ||||
chr11:65505194-65505854 | Common:1; Rare:313 | ||||
chr11:65652956-65653060 | Common:1; Rare:41 | ||||
chr11:66279857-66279982 | Common:2; Rare:23 | ||||
chr11:66346493-66346602 | Rare:36; Clinvar (benign):1 | ||||
chr11:66368992-66369108 | Rare:38 | ||||
chr11:67619774-67620011 | Common:5; Rare:50 | ||||
chr11:67805314-67805481 | Common:2; Rare:64 | ||||
chr11:70501905-70502119 | Rare:50 |