chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121004705210047053GA23GENIChomozygous50041191
121004706810047069AATATG12GENICheterozygous50529645
121004706810047069AATATGTATG12GENICpossibly homozygous50529647
121004749310047494AT17GENIChomozygous50041193
121004782810047832GTGT----1GENIChomozygous50529651
121004816910048170TA19GENIChomozygous50041197
121004817810048179CT16GENIChomozygous50041199
121004826110048262TC20GENIChomozygous50041201
121004863110048632AAAAT4GENIChomozygous50041204
121005944010059441CCTG3GENICheterozygous50529654
121005999710059998GC11GENIChomozygous50041206
121005999910060000GC12GENIChomozygous50041208
121006127210061273C-5GENIChomozygous50041210
121006130810061309TG8GENIChomozygous50041212
121006175810061759TG14GENICpossibly homozygous50041214
121006188010061881AG14GENIChomozygous50041216
121006228510062286AC11GENIChomozygous50041218
121006236110062362CT13GENIChomozygous50041220
121006252110062522CCGTGTGT16GENICheterozygous50041222
121006252110062522CCGTGT16GENICheterozygous50529657
121006280610062807CT28GENIChomozygous50041224
121006305010063051AG15GENIChomozygous50041226