chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193069835030698355AAAAA-----1GENIChomozygous46402056
193069835430698355AACGGG1GENIChomozygous46402058
193069927030699294TGCTGCTGCTGCTGCTGCTGCTGC------------------------3GENIChomozygous46636164
193070062430700625TC22GENIChomozygous46704683
193070634130706342TC29GENICpossibly homozygous46704684
193070839530708396TG23GENIChomozygous46704685
193070700330707005AC--13GENICheterozygous46507548
193070538930705390GA29GENIChomozygous46240571
193071472230714723CT27GENIChomozygous46704686
193071472630714727GGA26GENIChomozygous46704687
193071718130717182GGA10GENIChomozygous46704688
193071718230717183GGA10GENIChomozygous46704689
193071807030718071TC25GENIChomozygous46240574
193071849930718500GT31GENIChomozygous46704690
193071897030718971CCAGG20GENIChomozygous46487196
193071910030719101CCT3GENIChomozygous46429355
193071990530719906GA33GENIChomozygous46704691
193072259330722594CA19GENIChomozygous46704692
193072278430722785AT17GENICpossibly homozygous46704693
193072289130722892GA29GENICpossibly homozygous46704694
193072434330724344TC27GENICpossibly homozygous46240577
193072547430725476TC--30GENICpossibly homozygous46704695
193072127330721274TC37GENIChomozygous46487202