Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58278660-58278998 | Common:4; Rare:104 | ||||
chr19:58326875-58327051 | Common:1; Rare:42 | ||||
chr19:58327234-58327342 | Rare:26 | ||||
chr19:58440139-58440435 | Common:5; Rare:80 | ||||
chr19:58499206-58499545 | Common:2; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
chr19:58519763-58520011 | Rare:65 | ||||
chr19:58554927-58555262 | Common:2; Rare:119 | ||||
chr2:677364-677557 | Common:1; Rare:80 | ||||
chr2:3519483-3519628 | Common:2; Rare:51 | ||||
chr2:3558220-3558725 | Common:6; Rare:186 | ||||
chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9423163-9423302 | Common:1; Rare:30 | ||||
chr2:9423411-9423714 | Rare:96 | ||||
chr2:9474498-9474630 | Common:6; Rare:62 | ||||
chr2:9555664-9555966 | Common:2; Rare:101 |