Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44776429-44776783 | Rare:109 | ||||
chr1:44777612-44778146 | Common:2; Rare:132 | ||||
chr1:44808215-44808553 | Common:2; Rare:76 | ||||
chr1:45011921-45012269 | Common:5; Rare:96; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45326802-45326904 | Rare:19 | ||||
chr1:45339951-45340041 | Rare:33 | ||||
chr1:45340114-45340236 | Rare:53; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:45340381-45340566 | Common:1; Rare:47; Clinvar:1 | ||||
chr1:45500056-45500356 | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521688-45522093 | Common:1; Rare:142 | ||||
chr1:45550741-45551121 | Common:3; Rare:90 | ||||
chr1:45583931-45584114 | Rare:73 | ||||
chr1:45686432-45686655 | Rare:77 | ||||
chr1:45687036-45687357 | Common:2; Rare:84 | ||||
chr1:45688055-45688269 | Common:1; Rare:59 |