Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593529-63593675 | Rare:70; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:63593677-63593745 | Rare:30 | ||||
chr1:64841274-64841529 | Rare:56; Clinvar:1 | ||||
chr1:65148924-65149064 | Common:1; Rare:41 | ||||
chr1:65525621-65525810 | Rare:37 | ||||
chr1:66332121-66332475 | Rare:89 | ||||
chr1:66532660-66532933 | Common:3; Rare:58 | ||||
chr1:66533358-66533679 | Common:2; Rare:47 | ||||
chr1:66533849-66534182 | Common:2; Rare:81 | ||||
chr1:66924774-66925086 | Common:2; Rare:132 | ||||
chr1:66925149-66925518 | Common:2; Rare:116 | ||||
chr1:66930042-66930405 | Rare:122 | ||||
chr1:66958723-66958894 | Common:1; Rare:39 | ||||
chr1:67053643-67053769 | Common:4; Rare:53 | ||||
chr1:67053895-67054187 | Common:1; Rare:111 |