chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119167002119167003AT9GENICheterozygous54232460
7119167003119167004GT9GENICheterozygous54232462
7119167024119167025GC10GENIChomozygous54080648
7119168715119168716CT18GENICheterozygous54232464
7119169018119169019CT11GENICheterozygous54232466
7119171564119171565TC18GENIChomozygous54080649
7119172293119172294TC7GENIChomozygous54080650
7119172319119172320CCA3GENIChomozygous54080651
7119172339119172340AG11GENIChomozygous54080652
7119174257119174258TC19GENIChomozygous54080653
7119174763119174764CT22GENICheterozygous54920915
7119174765119174766TC23GENICheterozygous54232470
7119174880119174883TTT---7GENICheterozygous54080654
7119175645119175646GC14GENIChomozygous54232474
7119178334119178335CT15GENICheterozygous54232478
7119178360119178361CG17GENICheterozygous54232480
7119178506119178507TC20GENIChomozygous54080658
7119178786119178787CG19GENIChomozygous54080659
7119178787119178788CG19GENIChomozygous54080660
7119178986119178987C-22GENIChomozygous54080661
7119179253119179254AG18GENICheterozygous54232482
7119179428119179431TAT---14GENIChomozygous54080662
7119179450119179451TC15GENICheterozygous54232484
7119181047119181048TTAA9GENIChomozygous54080665
7119172976119172977GA23GENICheterozygous54750858
7119181427119181428GA11GENICheterozygous54750860