Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:34093690-34093861 | Rare:31 | ||||
chr20:35490929-35491052 | Rare:24 | ||||
chr20:36046654-36046985 | Common:1; Rare:73 | ||||
chr20:36049660-36050248 | Common:4; Rare:125 | ||||
chr20:36050254-36050314 | Rare:17 | ||||
chr20:36050322-36050737 | Common:2; Rare:145 | ||||
chr20:36064714-36064843 | Rare:33 | ||||
chr20:36548894-36549108 | Common:1; Rare:48 | ||||
chr20:36912459-36912669 | Rare:47; Clinvar (pathogenic):1 | ||||
chr20:40687640-40687894 | Rare:61; Clinvar:2; Clinvar (benign):3 | ||||
chr20:41092178-41092539 | Common:1; Rare:61 | ||||
chr20:45419361-45419586 | Common:2; Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr20:45470371-45470632 | Rare:93 | ||||
chr20:45899460-45899685 | Rare:77 | ||||
chr20:45909612-45909967 | Common:4; Rare:90 |