chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159931733159931734GA39GENICpossibly homozygous114073602
5159931790159931791GA43GENIChomozygous114073603
5159936882159936883TC40GENIChomozygous114073604
5159937645159937646TC26GENIChomozygous114073605
5159938134159938135TA52GENICheterozygous114073606
5159938314159938315TC34GENICpossibly homozygous114073607
5159938591159938592TC49GENIChomozygous114073608
5159939921159939922CT40GENIChomozygous114073609
5159940114159940115AG56GENIChomozygous114073610
5159940390159940391CT52GENIChomozygous114073611
5159940391159940392CA52GENIChomozygous114073612
5159940410159940411AG56GENICpossibly homozygous114073613
5159940919159940920AC64GENIChomozygous114073614
5159943138159943139TC28GENICheterozygous114073615
5159944166159944167AC6GENIChomozygous114073616
5159944581159944582GT52GENIChomozygous114073617
5159944742159944743GA43GENIChomozygous114073618
5159944930159944931CT57GENICpossibly homozygous114073619
5159945573159945574AC56GENIChomozygous114073620
5159945939159945940CA33GENIChomozygous114073621
5159945943159945944TA32GENIChomozygous114073622
5159945948159945949GA31GENIChomozygous114073623
5159945949159945950CT31GENIChomozygous114073624
5159945953159945954CT32GENICpossibly homozygous114073625
5159945991159945992CT54GENIChomozygous114073626