Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:74732994-74733326 | Common:6; Rare:115 | ||||
chr1:75732703-75732881 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:77219385-77219505 | Rare:54 | ||||
chr1:77888191-77888737 | Common:3; Rare:123; Clinvar:2 | ||||
chr1:77949210-77949411 | Rare:51; Clinvar:1 | ||||
chr1:77979025-77979298 | Common:2; Rare:90 | ||||
chr1:77979499-77979536 | Rare:12 | ||||
chr1:78004547-78004960 | Common:4; Rare:96 | ||||
chr1:84077904-84078176 | Common:1; Rare:96 | ||||
chr1:84506550-84506736 | Common:3; Rare:36 | ||||
chr1:84574025-84574128 | Common:1; Rare:19 | ||||
chr1:84574374-84574592 | Common:3; Rare:68 | ||||
chr1:84690387-84690706 | Rare:102 | ||||
chr1:84997064-84997204 | Common:6; Rare:41 | ||||
chr1:85259631-85259763 | Common:3; Rare:53 |