chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107627926776279268GA49GENIChomozygous116801270
107627937476279375GA38GENICpossibly homozygous117065911
107627995176279952GC96GENICheterozygous118124596
107627995876279959GA99GENICheterozygous118124597
107627998176279982GC106GENICheterozygous118124598
107628000076280001TC98GENICheterozygous118124599
107628002376280024GA90GENICheterozygous118124600
107628007576280076CT73GENICheterozygous118124601
107628022876280229AG58GENIChomozygous118124602
107628027176280272CA47GENIChomozygous118124603
107628036176280362TC48GENIChomozygous118124604
107628037076280371CA48GENIChomozygous118124605
107628045176280452CG37GENICheterozygous117086204
107628048176280482CT29GENICheterozygous118124606
107628073076280731AG46GENIChomozygous118124607
107628098476280985GT52GENICpossibly homozygous118124608