Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63523186-63523589 | Common:3; Rare:102 | ||||
chr1:63592956-63593476 | Rare:140; Clinvar (benign):1 | ||||
chr1:63593507-63593699 | Rare:95; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:64841233-64841529 | Rare:66; Clinvar:1 | ||||
chr1:66533389-66533659 | Common:2; Rare:41 | ||||
chr1:66533846-66534165 | Common:2; Rare:80 | ||||
chr1:66924810-66925035 | Rare:95 | ||||
chr1:66925207-66925514 | Common:2; Rare:97 | ||||
chr1:67053936-67054238 | Common:2; Rare:101 | ||||
chr1:67429989-67430605 | Rare:227 | ||||
chr1:68232468-68232673 | Rare:43 | ||||
chr1:70205542-70205778 | Rare:73 | ||||
chr1:70221296-70221591 | Rare:123 | ||||
chr1:70354674-70354852 | Rare:62 | ||||
chr1:70411069-70411297 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 |