Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1051583-1051784 | Rare:86; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:1115417-1115911 | Common:4; Rare:72 | ||||
chr1:1115994-1116413 | Common:2; Rare:411 | ||||
chr1:1185471-1185871 | Common:1; Rare:73 | ||||
chr1:1230913-1231660 | Common:4; Rare:252 | ||||
chr1:1231876-1232324 | Rare:592; Clinvar:11; Clinvar (benign):13; Clinvar (pathogenic):6 | ||||
chr1:1272747-1273180 | Common:5; Rare:205 | ||||
chr1:1273700-1274274 | Common:18; Rare:890 | ||||
chr1:1274315-1274715 | Rare:80 | ||||
chr1:1304629-1305060 | Common:4; Rare:220 | ||||
chr1:1305040-1305190 | Common:2; Rare:59 | ||||
chr1:1305520-1305870 | Common:1; Rare:220 | ||||
chr1:1307376-1307776 | Common:5; Rare:161 | ||||
chr1:1307813-1308704 | Common:62; Rare:1544 | ||||
chr1:1309694-1310110 | Common:7; Rare:333 |