Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62784069-62784180 | Rare:44 | ||||
chr1:63523186-63523589 | Common:3; Rare:102 | ||||
chr1:63593023-63593527 | Rare:148; Clinvar (benign):2 | ||||
chr1:63593659-63593675 | Rare:5; Clinvar (pathogenic):1 | ||||
chr1:64841224-64841529 | Rare:71; Clinvar:1 | ||||
chr1:65147466-65147653 | Rare:61 | ||||
chr1:65147938-65148305 | Common:5; Rare:79 | ||||
chr1:65148903-65149003 | Rare:27 | ||||
chr1:66332439-66332466 | Rare:12 | ||||
chr1:66533496-66533630 | Common:2; Rare:18 | ||||
chr1:66752329-66752494 | Rare:35 | ||||
chr1:66924835-66925046 | Rare:86 | ||||
chr1:66925207-66925518 | Common:2; Rare:98 | ||||
chr1:67053941-67054175 | Common:1; Rare:85 | ||||
chr1:67429991-67430467 | Rare:180 |