chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130556123130556124AG23GENIChomozygous115890580
7130556165130556166CT30GENIChomozygous115890582
7130556669130556670AG39GENIChomozygous115890584
7130556712130556713GT44GENIChomozygous115890586
7130556727130556728AT42GENIChomozygous115890588
7130556738130556739AG41GENIChomozygous115890590
7130557064130557065TC39GENIChomozygous115890592
7130557291130557292GA31GENIChomozygous115890594
7130557836130557837CT27GENIChomozygous115890596
7130558518130558519GA34GENIChomozygous115890598
7130558657130558658TC35GENIChomozygous115890600
7130558747130558748GT30GENIChomozygous115890602
7130558847130558848TC32GENIChomozygous115890604
7130559154130559155TC19GENIChomozygous115890606
7130559962130559963AG26GENIChomozygous115890608
7130559993130559994CA26GENIChomozygous115890609
7130560530130560531AG38GENIChomozygous115890611
7130560735130560736GA28GENIChomozygous115890613
7130561146130561147AG24GENIChomozygous115890615
7130561298130561299GA30GENIChomozygous115890619
7130561671130561672TC28GENIChomozygous115890621
7130561781130561782CT26GENIChomozygous115890623
7130561970130561971TC34GENIChomozygous115890625
7130562626130562627TG17GENIChomozygous116229653
7130562640130562641TA18GENIChomozygous116229654
7130563093130563094GA32GENIChomozygous116229655
7130563831130563832GC43GENIChomozygous115890627
7130563894130563895AC45GENIChomozygous116229657
7130564193130564194GC34GENIChomozygous115890629
7130564355130564356AT33GENIChomozygous115890631
7130564426130564427TA27GENIChomozygous116229660
7130564596130564597TC36GENIChomozygous115890633
7130564617130564618TC34GENIChomozygous115890635