Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61077018-61077406 | Common:3; Rare:93 | ||||
chr1:61082397-61082816 | Common:2; Rare:138 | ||||
chr1:61724987-61725202 | Rare:100 | ||||
chr1:62436255-62436399 | Common:2; Rare:46 | ||||
chr1:62437006-62437110 | Common:1; Rare:39 | ||||
chr1:62688279-62688536 | Common:1; Rare:92 | ||||
chr1:62784047-62784180 | Rare:50 | ||||
chr1:63367526-63367682 | Rare:46; Clinvar (benign):1 | ||||
chr1:63523170-63523589 | Common:3; Rare:110 | ||||
chr1:63592980-63593545 | Rare:165; Clinvar (benign):2 | ||||
chr1:63593656-63593689 | Rare:15; Clinvar (pathogenic):1 | ||||
chr1:63594186-63594282 | Common:3; Rare:22 | ||||
chr1:63773903-63774083 | Rare:32 | ||||
chr1:65147313-65147653 | Rare:87 | ||||
chr1:65147953-65148329 | Common:5; Rare:77 |