chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121004705210047053GA30GENIChomozygous50041191
121004706810047069AATATGTATG12GENIChomozygous50529647
121004749310047494AT23GENIChomozygous50041193
121004782810047832GTGT----2GENIChomozygous50529651
121004816910048170TA28GENIChomozygous50041197
121004817810048179CT27GENIChomozygous50041199
121004826110048262TC26GENIChomozygous50041201
121005944110059443TG--3GENICheterozygous50567952
121005999710059998GC15GENIChomozygous50041206
121005999910060000GC16GENIChomozygous50041208
121006127210061273C-11GENIChomozygous50041210
121006130810061309TG15GENIChomozygous50041212
121006175810061759TG25GENIChomozygous50041214
121006188010061881AG15GENIChomozygous50041216
121006228510062286AC13GENIChomozygous50041218
121006236110062362CT22GENIChomozygous50041220
121006252110062522CCGTGTGT15GENICpossibly homozygous50041222
121006252110062522CCGTGT15GENICheterozygous50529657
121006280610062807CT30GENIChomozygous50041224
121006305010063051AG19GENIChomozygous50041226