Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52055215-52055256 | Rare:12 | ||||
chr1:52056085-52056334 | Common:2; Rare:72 | ||||
chr1:52404490-52404637 | Common:1; Rare:47 | ||||
chr1:53238484-53238602 | Common:1; Rare:44 | ||||
chr1:53946271-53946398 | Rare:51 | ||||
chr1:54053188-54053697 | Common:6; Rare:164 | ||||
chr1:54199990-54200207 | Rare:45 | ||||
chr1:55215361-55215559 | Rare:75 | ||||
chr1:58546702-58546731 | Common:1; Rare:13 | ||||
chr1:62688254-62688533 | Common:1; Rare:107; Clinvar:1 | ||||
chr1:62784058-62784123 | Rare:22 | ||||
chr1:63322427-63322577 | Rare:47 | ||||
chr1:63523192-63523277 | Common:2; Rare:22 | ||||
chr1:63523407-63523579 | Rare:41 | ||||
chr1:63593339-63593683 | Rare:153; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 |