Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:71046742-71047256 | Common:1; Rare:157 | ||||
chr1:71080945-71081367 | Rare:112 | ||||
chr1:72282669-72282974 | Common:4; Rare:89 | ||||
chr1:74198148-74198338 | Common:2; Rare:108 | ||||
chr1:74732994-74733353 | Common:6; Rare:127 | ||||
chr1:75732708-75732854 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
chr1:76074560-76074876 | Common:2; Rare:103 | ||||
chr1:77219400-77219498 | Rare:45 | ||||
chr1:77888351-77888730 | Common:2; Rare:88; Clinvar:2 | ||||
chr1:77979008-77979298 | Common:2; Rare:102 | ||||
chr1:78004546-78004963 | Common:4; Rare:97 | ||||
chr1:78490747-78491149 | Common:2; Rare:88 | ||||
chr1:79006665-79006890 | Common:1; Rare:79 | ||||
chr1:84077942-84078171 | Common:1; Rare:79 | ||||
chr1:84506555-84506652 | Common:1; Rare:19 |