Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161314262-161314417 | Common:3; Rare:60; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161766176-161766382 | Common:3; Rare:69 | ||||
chr1:162023635-162023943 | Common:1; Rare:85 | ||||
chr1:162497735-162497859 | Common:1; Rare:36 | ||||
chr1:162561364-162561676 | Common:3; Rare:116 | ||||
chr1:162790496-162790793 | Common:4; Rare:84 | ||||
chr1:163203058-163203258 | Common:1; Rare:41 | ||||
chr1:163321713-163321964 | Common:1; Rare:68 | ||||
chr1:165768698-165768938 | Common:1; Rare:90; Clinvar:1 | ||||
chr1:166839292-166839530 | Rare:74 | ||||
chr1:166876234-166876462 | Rare:67 | ||||
chr1:166989218-166989297 | Rare:24 | ||||
chr1:167935880-167936255 | Common:1; Rare:104 | ||||
chr1:167936553-167936941 | Common:1; Rare:139 | ||||
chr1:167936997-167937126 | Rare:47 |