chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130556123130556124AG23GENIChomozygous115890580
7130556165130556166CT23GENIChomozygous115890582
7130556669130556670AG20GENIChomozygous115890584
7130556712130556713GT27GENIChomozygous115890586
7130556727130556728AT25GENIChomozygous115890588
7130556738130556739AG24GENIChomozygous115890590
7130557064130557065TC15GENIChomozygous115890592
7130557291130557292GA14GENIChomozygous115890594
7130557836130557837CT21GENIChomozygous115890596
7130558518130558519GA21GENIChomozygous115890598
7130558657130558658TC21GENIChomozygous115890600
7130558747130558748GT18GENIChomozygous115890602
7130558847130558848TC19GENIChomozygous115890604
7130559154130559155TC20GENIChomozygous115890606
7130559962130559963AG27GENIChomozygous115890608
7130559993130559994CA24GENIChomozygous115890609
7130560530130560531AG23GENIChomozygous115890611
7130560735130560736GA21GENIChomozygous115890613
7130561146130561147AG26GENIChomozygous115890615
7130561201130561202CT25GENIChomozygous115890617
7130561298130561299GA19GENIChomozygous115890619
7130559385130559386G23GENIChomozygous128520361
7130559746130559746GA22GENIChomozygous128520362
7130561671130561672TC21GENIChomozygous115890621
7130561781130561782CT17GENIChomozygous115890623
7130564193130564194GC21GENIChomozygous115890629
7130561970130561971TC19GENIChomozygous115890625
7130563831130563832GC21GENIChomozygous115890627
7130564355130564356AT27GENICpossibly homozygous115890631
7130564596130564597TC15GENIChomozygous115890633
7130564617130564618TC19GENIChomozygous115890635