Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593074-63593624 | Rare:188; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:63593632-63593699 | Rare:34; Clinvar (pathogenic):1 | ||||
chr1:64841243-64841529 | Rare:64; Clinvar:1 | ||||
chr1:65148965-65149064 | Common:1; Rare:30 | ||||
chr1:66332231-66332475 | Rare:69 | ||||
chr1:66533546-66533606 | Rare:6 | ||||
chr1:66924838-66925031 | Rare:83 | ||||
chr1:66925220-66925503 | Common:2; Rare:91 | ||||
chr1:67429989-67430344 | Rare:120 | ||||
chr1:70205536-70205762 | Rare:74 | ||||
chr1:70354705-70354827 | Rare:42 | ||||
chr1:70411053-70411268 | Common:1; Rare:52; Clinvar:1 | ||||
chr1:71080956-71081373 | Rare:110 | ||||
chr1:72282669-72282961 | Common:4; Rare:78 | ||||
chr1:74198148-74198331 | Common:2; Rare:107 |