chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145119351145119352AG20GENIChomozygous115946571
7145120078145120079TG21GENIChomozygous115946573
7145120692145120693CA34GENIChomozygous115946575
7145120839145120840CT26GENIChomozygous115946577
7145121810145121811TG22GENIChomozygous115946582
7145121814145121815TC22GENIChomozygous115946584
7145121834145121835CG24GENIChomozygous115946586
7145121967145121968GT23GENIChomozygous115946588
7145122094145122095GA42GENIChomozygous115946590
7145124175145124176AG19GENIChomozygous115946593
7145124844145124845GA21GENIChomozygous115946595
7145125788145125789AG24GENIChomozygous115946597
7145125874145125875GA21GENIChomozygous115946599
7145126437145126438GA19GENIChomozygous115946601
7145130955145130956GA14GENIChomozygous115946607
7145131424145131425GA20GENICpossibly homozygous115946609
7145134037145134038GT19GENIChomozygous115946611
7145135727145135728GA27GENIChomozygous115946613
7145136230145136231GA26GENIChomozygous115946614
7145145016145145017CT15GENIChomozygous115946616