Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262415-160262636 | Common:1; Rare:68 | ||||
chr1:160343181-160343421 | Rare:100 | ||||
chr1:160400348-160400615 | Common:1; Rare:64 | ||||
chr1:161021021-161021443 | Common:5; Rare:113 | ||||
chr1:161045888-161046057 | Common:1; Rare:44 | ||||
chr1:161117995-161118141 | Rare:77 | ||||
chr1:161132415-161132692 | Common:1; Rare:93 | ||||
chr1:161159392-161159555 | Common:1; Rare:51 | ||||
chr1:161314201-161314417 | Common:3; Rare:80; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161750264-161750456 | Rare:34 | ||||
chr1:161766157-161766407 | Common:3; Rare:83 | ||||
chr1:162497761-162497859 | Common:1; Rare:33 | ||||
chr1:162561351-162561705 | Common:4; Rare:135 | ||||
chr1:162790516-162790789 | Common:4; Rare:79 | ||||
chr1:163321727-163321964 | Common:1; Rare:65 |