Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593030-63593490 | Rare:132; Clinvar (benign):1 | ||||
chr1:63593510-63593980 | Common:4; Rare:198; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:63773770-63774270 | Rare:100 | ||||
chr1:64505170-64505570 | Common:6; Rare:129 | ||||
chr1:64663690-64664020 | Common:1; Rare:88 | ||||
chr1:64664420-64664666 | Common:1; Rare:66 | ||||
chr1:64744750-64745310 | Common:3; Rare:156 | ||||
chr1:64966468-64966773 | Common:3; Rare:114 | ||||
chr1:65147380-65147700 | Common:1; Rare:89 | ||||
chr1:65254337-65254463 | Common:2; Rare:47 | ||||
chr1:65419843-65420273 | Common:2; Rare:123 | ||||
chr1:65420333-65420682 | Common:4; Rare:82; Clinvar:1 | ||||
chr1:65792618-65793558 | Common:3; Rare:252 | ||||
chr1:65992281-65992849 | Common:1; Rare:135 | ||||
chr1:66331713-66331818 | Rare:20 |