chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117817276378172764AG17GENIChomozygous50834989
117817284178172845AAAC----6GENIChomozygous50834990
117817371378173714G-6GENICheterozygous50895433
117818272778182729AC--9GENICpossibly homozygous50834993
117818311578183116CT3GENIChomozygous50834994
117818322578183226GGC12GENICpossibly homozygous50834995
117818449478184495CCA1GENIChomozygous51190308
117818742378187446GGTGGTGCTACACCAAGAGGAGA-----------------------1GENIChomozygous50834997
117818773378187734CT10GENIChomozygous50834999
117818804078188041TC28GENIChomozygous50835000
117818841178188412TC6GENIChomozygous50835002
117818861878188619GGC3GENIChomozygous50835004
117818906078189061GA17GENIChomozygous50835005
117818910078189101AAT7GENICpossibly homozygous50835006
117818911678189117CT8GENIChomozygous50835007
117818923578189236CT18GENICpossibly homozygous50835008
117818932178189322AG16GENICpossibly homozygous50835009