Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70221321-70221530 | Rare:88 | ||||
chr1:70354682-70354883 | Rare:64 | ||||
chr1:70411027-70411297 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080996-71081393 | Rare:108 | ||||
chr1:74198148-74198265 | Common:1; Rare:61 | ||||
chr1:74733025-74733266 | Common:5; Rare:77 | ||||
chr1:75724277-75724598 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
chr1:76074634-76074859 | Rare:63 | ||||
chr1:77219398-77219490 | Rare:42 | ||||
chr1:77683331-77683664 | Common:1; Rare:103 | ||||
chr1:77888270-77888600 | Common:3; Rare:66 | ||||
chr1:77978987-77979313 | Common:2; Rare:115 | ||||
chr1:78004552-78004873 | Common:3; Rare:80 | ||||
chr1:81800240-81800386 | Common:1; Rare:47 | ||||
chr1:84077943-84078176 | Common:1; Rare:80 |