Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54199974-54200276 | Rare:88 | ||||
chr1:54887035-54887103 | Rare:23; Clinvar (benign):1 | ||||
chr1:54887155-54887366 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
chr1:55215338-55215406 | Rare:31 | ||||
chr1:56645177-56645460 | Common:1; Rare:93 | ||||
chr1:59296520-59296857 | Common:12; Rare:91 | ||||
chr1:61076970-61077233 | Common:3; Rare:70 | ||||
chr1:61725109-61725456 | Common:2; Rare:111 | ||||
chr1:61742211-61742505 | Rare:70 | ||||
chr1:62436832-62437102 | Common:1; Rare:67 | ||||
chr1:62437130-62437279 | Common:1; Rare:37 | ||||
chr1:62688283-62688513 | Rare:82 | ||||
chr1:62784073-62784191 | Rare:50 | ||||
chr1:63322440-63322759 | Common:2; Rare:95 | ||||
chr1:63523171-63523581 | Common:3; Rare:108 |