chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56305850163058502TG45GENICheterozygous55422511
56307001863070019GC43GENICpossibly homozygous56017539
56307186063071861CT63GENICheterozygous55422541
56307187163071872AT72GENICheterozygous55422543
56307194663071947TG59GENICheterozygous55422545
56307291563072916CG64GENICheterozygous55879893
56308238263082384TG--28GENICheterozygous55422563
56308411963084120G-9GENICheterozygous55422569
56308716063087161T-2GENIChomozygous55879899
56309116763091168T-15GENIChomozygous55422590
56309117363091174TC12GENIChomozygous55422592
56309117563091176TA12GENIChomozygous55422594
56309118363091184TC10GENIChomozygous55422596
56309161563091616GT36GENICheterozygous55422598
56310962863109629GGTCTT18GENICpossibly homozygous55422612
56310968963109690TTC29GENICheterozygous55422618
56311322363113224CG26GENICpossibly homozygous55422636
56311325163113252CT30GENIChomozygous55422638
56311612963116130CA111GENICheterozygous55422648
56311781663117817GA53GENICheterozygous55422652
56311786763117868AG65GENICheterozygous55422654
56311789463117895TC71GENICheterozygous55422656
56311798363117984AG64GENICheterozygous55422658
56311800963118010TC55GENICheterozygous55422660
56311803963118040C-43GENICheterozygous55422668