chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142185688721856888CT51GENIChomozygous139475758
142185726321857264TC39GENIChomozygous139475759
142185744321857444AG40GENIChomozygous139475761
142185801621858017GT43GENIChomozygous139475762
142185846321858464AG50GENIChomozygous139475763
142185920321859204AG41GENIChomozygous139475764
142185959121859592GA43GENIChomozygous142437207
142186131821861319CT17GENIChomozygous142437208
142186138021861381GA10GENICheterozygous404481885
142186138021861381GC10GENICheterozygous404481886
142186138021861381G10GENICpossibly homozygous404481887
142186067421860675AG52GENICpossibly homozygous146555792
142186138821861389GC10GENICheterozygous403354575
142186138821861389GA10GENICheterozygous403354576
142186191021861911AG32GENIChomozygous139475767
142186217621862177GA37GENIChomozygous142437209
142186371521863716CT38GENIChomozygous142437210
142186464321864644CT33GENICpossibly homozygous142437211
142186759521867596TA25GENIChomozygous142437212
142186817321868174GT29GENIChomozygous142437213
142186827921868280CT40GENIChomozygous142437214
142187030321870304AG37GENIChomozygous139475775
142187071321870714GA36GENIChomozygous142437215
142187084421870845TC52GENIChomozygous142437216
142187109821871099AG40GENIChomozygous142437217
142187134821871349GA49GENIChomozygous142437218
142187435521874356AT42GENIChomozygous139475788
142187454121874541A37GENICpossibly homozygous139384737
142186169121861692C26GENIChomozygous142419853
142186816921868170G29GENIChomozygous142419854
142186997521869975ACACTTCCGGGCAAGGAC40GENIChomozygous139384733
142187221721872217CCTGACCACGGAACCTCA43GENIChomozygous139384735
142186139021861391GC10GENICheterozygous147802013
142187470821874709TC29GENIChomozygous139475792