chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174172215741722158CCGTGTGT12GENICpossibly homozygous724962617
174172468941724690CT29GENIChomozygous593861575
174172552441725525CT27GENIChomozygous593861576
174172563841725639GT28GENIChomozygous593861577
174172621341726215AG--12GENIChomozygous724962618
174172672241726723TC31GENIChomozygous593861578
174173011141730112GGATAT34GENIChomozygous724962619
174173011241730113CCTCTAGA34GENIChomozygous724962620
174173071941730720GT35GENIChomozygous593861579
174173079441730795TC35GENIChomozygous593861580