chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72396151123961512TC36GENICpossibly homozygous775797716
72396156523961566CT33GENICheterozygous775797717
72396157523961576CT35GENICheterozygous775797718
72396297123962972AG36GENIChomozygous775797719
72396300923963010AC43GENIChomozygous775797720
72396304123963042GT42GENIChomozygous775797721
72396808323968084TA79GENIChomozygous775797722
72396809323968094AC65GENIChomozygous775797723
72396809623968097GT64GENICpossibly homozygous775797724
72396846723968468AT37GENIChomozygous775797725
72396882223968823TC30GENIChomozygous775797726
72397297723972978AG29GENICpossibly homozygous775797727
72397355123973552AG38GENIChomozygous775797728
72397444223974443AG22GENIChomozygous775797729
72397463123974632GA46GENICpossibly homozygous775797730
72397638723976388TC60GENIChomozygous775797731
72398050123980502GA53GENIChomozygous775797732
72398120923981210TC57GENIChomozygous775797733
72398280023982801GA38GENIChomozygous775797734
72398282323982824CT41GENIChomozygous775797735
72398487523984876TC53GENIChomozygous775797736
72398499623984997TC63GENIChomozygous775797737
72398522323985224TC47GENIChomozygous775797738