Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154272408-154272848 | Common:4; Rare:117; Clinvar:3; Clinvar (benign):4 | ||||
chr1:154325370-154325701 | Rare:114 | ||||
chr1:154327600-154327785 | Rare:44 | ||||
chr1:154501434-154501656 | Common:1; Rare:73 | ||||
chr1:154501724-154501891 | Rare:59 | ||||
chr1:154502353-154502498 | Common:2; Rare:38 | ||||
chr1:154502843-154502977 | Common:2; Rare:41 | ||||
chr1:154558244-154558512 | Rare:79 | ||||
chr1:154558607-154559092 | Common:2; Rare:139 | ||||
chr1:154608021-154608255 | Rare:75; Clinvar (benign):1 | ||||
chr1:154627864-154628039 | Common:3; Rare:88 | ||||
chr1:154936838-154937227 | Rare:82 | ||||
chr1:154956012-154956236 | Common:1; Rare:62 | ||||
chr1:154961365-154961560 | Rare:60 | ||||
chr1:154961669-154961855 | Common:1; Rare:73 |