Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25549075-25549475 | Common:4; Rare:66 | ||||
chr1:25549510-25550036 | Common:21; Rare:299 | ||||
chr1:25550083-25550392 | Common:1; Rare:58 | ||||
chr1:25799800-25800280 | Common:3; Rare:354; Clinvar:14; Clinvar (benign):22; Clinvar (pathogenic):4 | ||||
chr1:25800300-25800640 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr1:25818483-25818883 | Common:3; Rare:74 | ||||
chr1:25819074-25819478 | Common:31; Rare:147 | ||||
chr1:25819670-25820260 | Common:35; Rare:716 | ||||
chr1:25820630-25821275 | Common:19; Rare:454 | ||||
chr1:25821351-25822048 | Common:3; Rare:215 | ||||
chr1:25859292-25859807 | Common:24; Rare:910 | ||||
chr1:25905345-25905774 | Common:4; Rare:467 | ||||
chr1:25905901-25906301 | Rare:182 | ||||
chr1:25906310-25906750 | Rare:528 | ||||
chr1:25997047-25998473 | Common:23; Rare:889 |