chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108897976988979770CT4GENIChomozygous51730995
108898078488980808CTCCTCCTCCTCCTCCTCCTCCTT------------------------2GENIChomozygous52394248
108898129688981302GAGGGA------10GENIChomozygous51730997
108898204288982043TC10GENIChomozygous51730999
108898273988982740AG28GENIChomozygous51731001
108898330188983305CCCC----18GENIChomozygous51536487
108898372988983735ACACAA------20GENICpossibly homozygous51731005
108898458488984585CG12GENIChomozygous51731009
108898529488985295CT22GENIChomozygous51731011
108898564388985644CCT11GENICheterozygous52394250
108898564488985647CTT---11GENICheterozygous51731013
108898614888986149CCT4GENICheterozygous52394252
108898614888986149CCTTT4GENICheterozygous52650830
108898702388987024AATG20GENIChomozygous51731015
108898709588987096C-10GENIChomozygous52322999
108898710088987107CTCTCTC-------2GENIChomozygous52394254
108898745588987456TC22GENIChomozygous51731017
108898800888988009CT19GENIChomozygous51731019
108899200788992008CCTTTTTT10GENICheterozygous52394256
108899220388992204A-15GENICpossibly homozygous51536494
108899242788992428CT27GENIChomozygous51731021
108899244988992450T-15GENIChomozygous51731023
108899308988993090TA29GENIChomozygous51731025
108899347688993478TT--7GENIChomozygous51731027
108899408088994081TC27GENIChomozygous51731029
108899521688995217AG22GENIChomozygous51731031