chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145119351145119352AG20GENIChomozygous115946571
7145120078145120079TG33GENIChomozygous115946573
7145120692145120693CA29GENIChomozygous115946575
7145120839145120840CT29GENIChomozygous115946577
7145121810145121811TG24GENIChomozygous115946582
7145121814145121815TC24GENIChomozygous115946584
7145121834145121835CG23GENIChomozygous115946586
7145121967145121968GT27GENIChomozygous115946588
7145122094145122095GA28GENIChomozygous115946590
7145124175145124176AG23GENIChomozygous115946593
7145124844145124845GA23GENIChomozygous115946595
7145125788145125789AG20GENIChomozygous115946597
7145125874145125875GA30GENIChomozygous115946599
7145126437145126438GA18GENIChomozygous115946601
7145129161145129162AG15GENIChomozygous115946605
7145130955145130956GA19GENIChomozygous115946607
7145131424145131425GA21GENIChomozygous115946609
7145132648145132649GT6GENIChomozygous118261264
7145135727145135728GA20GENIChomozygous115946613
7145136230145136231GA30GENIChomozygous115946614
7145145016145145017CT19GENIChomozygous115946616