Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:71080992-71081367 | Rare:100 | ||||
chr1:72282844-72282906 | Common:2; Rare:15 | ||||
chr1:74198149-74198356 | Common:2; Rare:115 | ||||
chr1:74732980-74733323 | Common:6; Rare:117 | ||||
chr1:77219400-77219520 | Rare:54 | ||||
chr1:77888092-77888388 | Common:1; Rare:68 | ||||
chr1:77888410-77888756 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77917963-77918268 | Common:1; Rare:83; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:77926483-77926888 | Common:1; Rare:118; Clinvar:15; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr1:77947806-77947892 | Rare:17 | ||||
chr1:77979026-77979340 | Common:3; Rare:100 | ||||
chr1:77979468-77979551 | Common:1; Rare:25 | ||||
chr1:78004552-78004971 | Common:4; Rare:94 | ||||
chr1:84506555-84506723 | Common:3; Rare:31 | ||||
chr1:84690372-84690691 | Rare:98 |