chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103169443931694440GT72GENICheterozygous117076343
103169766331697664GA67GENICpossibly homozygous116976878
103169833531698336CT50GENICpossibly homozygous117193931
103169837331698374AC50GENICpossibly homozygous117986799
103169837931698380AC52GENICpossibly homozygous117986800
103169838531698386AC54GENICpossibly homozygous117986801
103169841331698414AC58GENICheterozygous117217198
103169938931699390TC61GENICheterozygous117986802
103170008131700082GA48GENIChomozygous117076344
103170076131700762TC59GENIChomozygous116547232
103169577031695771AG64GENIChomozygous116547226
103170094031700941TG51GENIChomozygous116547234
103170223831702239CT78GENIChomozygous116547236
103170243931702440AC62GENICpossibly homozygous116547238
103170282331702824AC97GENIChomozygous116547240
103170604631706047AC85GENICheterozygous117986803
103170607731706078GT95GENICheterozygous117986804
103170609031706091TC89GENICheterozygous117986805
103170628131706282TC124GENIChomozygous116752786
103170788031707881CT43GENIChomozygous116547244
103170788931707890CT42GENIChomozygous116547246
103170839931708400GA71GENIChomozygous117217200
103170971631709717GA51GENIChomozygous116547248
103171076531710766AC65GENICheterozygous117986806
103171082831710829CT69GENICheterozygous117986808
103171083931710840CT69GENICheterozygous117986809
103171084031710841AG68GENICheterozygous117986810
103171084331710844AG69GENICheterozygous117986811
103171084931710850AG75GENICheterozygous117986812
103171087831710879TC65GENICheterozygous117986813
103171089031710891AG60GENICheterozygous117986814
103171184231711843CT45GENIChomozygous116547250
103170635131706352GA82GENICheterozygous118034428
103171078231710783AG65GENICheterozygous118034429
103171078531710786AG64GENICheterozygous118034430
103171194131711942GC35GENIChomozygous118034431