chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117459668874596689AG30GENIChomozygous50962130
117459742574597426AG6GENIChomozygous50962131
117459850674598507AT16GENIChomozygous51284763
117459855974598560G-22GENIChomozygous51125830
117459914574599151ACAGTA------3GENIChomozygous51189148
117460028074600281GA17GENIChomozygous51125832
117460092174600922CCAAGAGAACCTCAAA25GENIChomozygous51125835
117460109774601098CT29GENICpossibly homozygous51125838
117460152774601528AG26GENIChomozygous51125841
117460175074601751AAGAAG15GENIChomozygous51284764
117460300874603009CT17GENIChomozygous51125847
117460330874603309CT12GENIChomozygous51588246
117460351374603530TTTTTTTTTTTTTTTTT-----------------8GENICheterozygous51284766
117460680574606806GC23GENIChomozygous51588250
117460484974604850AG17GENIChomozygous51588248
117460509074605091T-10GENICpossibly homozygous50832331
117460521174605212AG17GENIChomozygous50832332
117460689374606894AAAAAG10GENIChomozygous51125861
117460720574607210GAAAA-----12GENIChomozygous50992511