chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108897976988979770CT2GENIChomozygous51730995
108898078488980808CTCCTCCTCCTCCTCCTCCTCCTT------------------------2GENIChomozygous52394248
108898129688981302GAGGGA------4GENIChomozygous51730997
108898204288982043TC6GENIChomozygous51730999
108898273988982740AG17GENIChomozygous51731001
108898372988983735ACACAA------20GENICpossibly homozygous51731005
108898458488984585CG7GENIChomozygous51731009
108898529488985295CT18GENIChomozygous51731011
108898564488985647CTT---7GENIChomozygous51731013
108898614888986149CCT7GENICheterozygous52394252
108898614888986149CCTTT7GENICheterozygous52650830
108898702388987024AATG24GENICpossibly homozygous51731015
108898330188983305CCCC----15GENIChomozygous51536487
108898709588987096C-15GENIChomozygous52322999
108898710088987107CTCTCTC-------1GENIChomozygous52394254
108898745588987456TC12GENIChomozygous51731017
108898800888988009CT18GENIChomozygous51731019
108899200788992008CCTTTTTT9GENICheterozygous52394256
108899202788992034GTTGCTG-------17GENICheterozygous52462168
108899220388992204A-6GENIChomozygous51536494
108899242788992428CT19GENIChomozygous51731021
108899244988992450T-13GENIChomozygous51731023
108899308988993090TA16GENIChomozygous51731025
108899347688993478TT--4GENIChomozygous51731027
108899408088994081TC10GENIChomozygous51731029
108899521688995217AG11GENIChomozygous51731031