Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61742369-61742553 | Rare:54 | ||||
chr1:62436253-62436385 | Common:2; Rare:41 | ||||
chr1:62436981-62437110 | Common:1; Rare:42 | ||||
chr1:62688260-62688510 | Common:1; Rare:100; Clinvar:1 | ||||
chr1:62784047-62784185 | Rare:54 | ||||
chr1:63523170-63523581 | Common:3; Rare:108 | ||||
chr1:63593648-63593675 | Rare:10; Clinvar (pathogenic):1 | ||||
chr1:64841243-64841574 | Rare:78; Clinvar:2 | ||||
chr1:65148903-65149051 | Common:1; Rare:46 | ||||
chr1:66924845-66925036 | Rare:80 | ||||
chr1:66930088-66930411 | Rare:100 | ||||
chr1:67429965-67430127 | Rare:59 | ||||
chr1:67430131-67430491 | Rare:136 | ||||
chr1:67833319-67833487 | Common:2; Rare:68 | ||||
chr1:68232429-68232635 | Common:1; Rare:48 |