chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117817276378172764AG18GENIChomozygous50834989
117817284178172845AAAC----7GENIChomozygous50834990
117817874878178749CG20GENICpossibly homozygous51146945
117818272778182729AC--14GENICpossibly homozygous50834993
117818311578183116CT2GENICheterozygous50834994
117818322578183226GGC14GENIChomozygous50834995
117818700678187007GA11GENIChomozygous50895567
117818742378187446GGTGGTGCTACACCAAGAGGAGA-----------------------2GENIChomozygous50834997
117818773378187734CT10GENICheterozygous50834999
117818804078188041TC25GENICpossibly homozygous50835000
117818841178188412TC6GENIChomozygous50835002
117818861878188619GGC8GENIChomozygous50835004
117818906078189061GA25GENICpossibly homozygous50835005
117818910078189101AAT5GENICheterozygous50835006
117818910078189101AATT5GENICheterozygous50895587
117818911678189117CT8GENIChomozygous50835007
117818923578189236CT13GENICpossibly homozygous50835008
117818932178189322AG18GENICheterozygous50835009