chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187656987776569878AG2GENIChomozygous131213583
187658383776583838CT4GENIChomozygous131213584
187658389176583892GT3GENIChomozygous129575222
187658389376583894AG3GENIChomozygous129575223
187658411776584118CT1GENIChomozygous129575224
187661448176614482GT21GENIChomozygous110409540
187661518076615181GA11GENIChomozygous110732933
187661823276618232C3GENIChomozygous129554753
187661825476618254C1GENIChomozygous129554754
187661827176618272TC1GENIChomozygous119502329
187661971976619720AG25GENIChomozygous110409542
187662039276620392T18GENICpossibly homozygous129554756
187662118576621186AT16GENIChomozygous110409544
187662130576621306AG12GENIChomozygous110601396
187662177276621773AG32GENIChomozygous110409546
187662285076622851TC18GENIChomozygous110409548
187662290076622901CA20GENIChomozygous110732935
187662295576622956TC19GENIChomozygous110409550
187662328876623289TC24GENIChomozygous110732937
187662513076625131TA24GENIChomozygous110409554
187662566076625661CT30GENIChomozygous110732939
187662674976626750TA20GENIChomozygous110409556
187662769376627694GA22GENIChomozygous110732941
187662770776627708TG20GENIChomozygous110409560
187662376576623766T13GENIChomozygous131209628
187662641176626411AAAAC15GENIChomozygous131209629