chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145118052145118053GA33GENIChomozygous115946569
7145119351145119352AG55GENIChomozygous115946571
7145120078145120079TG49GENIChomozygous115946573
7145120692145120693CA32GENIChomozygous115946575
7145120839145120840CT30GENIChomozygous115946577
7145121012145121013CT36GENICheterozygous115946578
7145121171145121172TC45GENIChomozygous115946580
7145121810145121811TG58GENIChomozygous115946582
7145121814145121815TC59GENIChomozygous115946584
7145121834145121835CG53GENIChomozygous115946586
7145121967145121968GT39GENIChomozygous115946588
7145122094145122095GA36GENICpossibly homozygous115946590
7145123742145123743AT28GENIChomozygous115946591
7145124175145124176AG57GENIChomozygous115946593
7145124844145124845GA38GENICpossibly homozygous115946595
7145125788145125789AG53GENIChomozygous115946597
7145125874145125875GA40GENIChomozygous115946599
7145126437145126438GA56GENICpossibly homozygous115946601
7145128606145128607TC20GENIChomozygous115946603
7145129161145129162AG25GENIChomozygous115946605
7145130955145130956GA48GENICpossibly homozygous115946607
7145131424145131425GA46GENIChomozygous115946609
7145134037145134038GT43GENIChomozygous115946611
7145135727145135728GA46GENIChomozygous115946613
7145136230145136231GA59GENIChomozygous115946614
7145145016145145017CT42GENIChomozygous115946616