chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119167002119167003AT23GENIChomozygous54232460
7119167003119167004GT23GENIChomozygous54232462
7119167024119167025GC25GENIChomozygous54080648
7119168715119168716CT26GENIChomozygous54232464
7119169018119169019CT24GENIChomozygous54232466
7119171564119171565TC25GENIChomozygous54080649
7119172293119172294TC14GENICpossibly homozygous54080650
7119172319119172320CCA8GENIChomozygous54080651
7119172339119172340AG17GENIChomozygous54080652
7119174117119174118CCT12GENIChomozygous54232468
7119174257119174258TC22GENIChomozygous54080653
7119174882119174883T-10GENIChomozygous54232472
7119175645119175646GGC3GENICheterozygous54080656
7119175645119175646GC7GENIChomozygous54232474
7119177325119177327TT--18GENICpossibly homozygous54232476
7119177326119177327T-18GENICheterozygous54080657
7119178334119178335CT23GENIChomozygous54232478
7119178360119178361CG27GENIChomozygous54232480
7119178506119178507TC32GENIChomozygous54080658
7119178786119178787CG28GENIChomozygous54080659
7119178787119178788CG28GENIChomozygous54080660
7119178986119178987C-26GENIChomozygous54080661
7119179253119179254AG33GENIChomozygous54232482
7119179428119179431TAT---23GENIChomozygous54080662
7119179450119179451TC24GENIChomozygous54232484
7119180205119180206C-11GENIChomozygous54232486
7119180586119180587TC44GENIChomozygous54080664
7119181047119181048TTAA28GENIChomozygous54080665