chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77159982371599824TC41GENICpossibly homozygous115710635
77161713471617135GC38GENIChomozygous115710646
77161714571617146CA55GENIChomozygous115710647
77161778771617788GT48GENIChomozygous115710651
77161720771617208GA63GENIChomozygous115710648
77161731571617316CT25GENIChomozygous115710649
77161769971617700AC34GENIChomozygous115710650
77161783371617834AC48GENICpossibly homozygous115710652
77161959971619600AC53GENICheterozygous116291695
77163297471632975TG2GENIChomozygous116033995
77163900771639008TG60GENIChomozygous116191806
77163930871639309TA68GENICheterozygous116034015
77163931171639312GA70GENICheterozygous116034017
77163932271639323CT70GENICheterozygous116034019
77163932771639328AG72GENICheterozygous116034021
77167479671674797AG60GENIChomozygous115710819
77168564071685641TC51GENIChomozygous115710856
77168565371685654GA50GENIChomozygous115710857