chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153962395939623960GA3GENIChomozygous112483797
153962429739624298CT17GENIChomozygous112483799
153962588439625885CG20GENIChomozygous112483801
153962788639627887AT20GENIChomozygous112483803
153962845439628455GT14GENICpossibly homozygous118956014
153963523939635240CT9GENICpossibly homozygous118914547
153963526439635265TC6GENIChomozygous118914548
153963528839635289AC9GENIChomozygous118914549
153963533039635331CT12GENIChomozygous112672826
153963533139635332GA12GENIChomozygous112483805
153963557339635574TA4GENIChomozygous112483807
153963659739636598CA14GENIChomozygous112914108
153963681239636813TG18GENIChomozygous112483809
153964112139641122GA13GENIChomozygous113079199
153964299439642995AT35GENIChomozygous112483813
153964511339645114TC25GENIChomozygous112483815
153964575539645756TC31GENIChomozygous112483817
153964767239647673CA19GENIChomozygous112483819
153965159539651596CT16GENIChomozygous112483821
153965227739652278CT16GENIChomozygous112483823
153965400939654010AG32GENIChomozygous112483825
153965868739658688AG26GENIChomozygous112483827
153965956139659562CA20GENIChomozygous112483829
153966452939664530GA32GENICheterozygous112483831
153966459339664594TA35GENICheterozygous113070408
153966456939664570AG39GENICheterozygous113070406
153966458939664590CT34GENICheterozygous113070407
153966467839664679GA29GENICheterozygous118956019
153966468639664687GC25GENICheterozygous118956020
153966475539664756CA41GENICheterozygous112988119
153966477539664776GA40GENICheterozygous112483833
153966479939664800TC46GENICheterozygous112988121
153966485239664853CG60GENICheterozygous113140592
153966490339664904CA44GENICheterozygous113278641
153966490939664910TC45GENICheterozygous113278643
153966492139664922GA49GENICheterozygous118914554
153966492639664927CT47GENICheterozygous118914555
153966493639664937TA44GENICheterozygous118914556
153966495239664953CT38GENICheterozygous118914557
153966497339664974TA35GENICheterozygous118914558