chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3120733152120733153GA60GENIChomozygous119800574
3120733420120733421TA49GENIChomozygous111689064
3120734394120734395TC61GENIChomozygous119800576
3120735447120735448AT53GENIChomozygous111689065
3120736466120736467AG59GENIChomozygous111689067
3120736650120736651TC52GENIChomozygous111689068
3120737212120737213GA56GENIChomozygous111689070
3120737424120737425GA32GENICpossibly homozygous132962982
3120737426120737427GA35GENICheterozygous132962983
3120738341120738341T46GENICpossibly homozygous130909976
3120738767120738768CT55GENIChomozygous111689077
3120739907120739907C67GENIChomozygous130909977
3120738780120738781TA60GENIChomozygous119800578
3120739178120739179AG36GENIChomozygous132962984
3120740540120740541GA74GENIChomozygous119800580
3120742893120742894GA51GENIChomozygous119800582
3120744849120744850GT39GENIChomozygous119800584
3120745697120745698GT58GENICpossibly homozygous119800586
3120747098120747099AT20GENIChomozygous119800590
3120747873120747874CG51GENIChomozygous132962985
3120749917120749918TC53GENIChomozygous111689079
3120751261120751262GT48GENICpossibly homozygous119800592
3120751897120751898TG56GENIChomozygous111689080
3120752225120752226CT52GENIChomozygous119800594
3120754107120754108AG55GENIChomozygous111689081
3120755902120755903GA56GENIChomozygous119800597
3120756338120756339T62GENIChomozygous132957304
3120757496120757497AG56GENIChomozygous112143441
3120757679120757680AG29GENIChomozygous111689082
3120757724120757725AG17GENIChomozygous112143443
3120759531120759531GTCCGAATCTCAGTGACTGTGACTGGCAGTAAAGG62GENIChomozygous127924464
3120759679120759680AG60GENIChomozygous112143449
3120759713120759715GT51GENIChomozygous132957305
3120759729120759730AC53GENIChomozygous112143450
3120759978120759979CT64GENIChomozygous119800601
3120760930120760931AG48GENIChomozygous112143451
3120761495120761496GA26GENIChomozygous119685263
3120763480120763481AG58GENIChomozygous111689086
3120763673120763673AAAA50GENIChomozygous127924465