chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17138091471380915GA17GENIChomozygous109104368
17138350671383507GA13GENIChomozygous108863481
17138583671385837AG15GENIChomozygous108863491
17138636171386362CT13GENIChomozygous109104372
17138714271387143TC13GENIChomozygous108863493
17138801471388015TA15GENIChomozygous109104374
17138855471388555CT12GENIChomozygous109104376
17138910471389105TC14GENIChomozygous108863497
17138989871389899GA19GENIChomozygous109104378
17139028371390284CT16GENIChomozygous109104380
17139257271392573AG19GENIChomozygous108863506
17139389071393891TC17GENIChomozygous108863512
17139408471394085GC16GENIChomozygous108863513
17139499471394995CT18GENIChomozygous108863519
17139578471395785CT9GENIChomozygous108863520
17139595571395956TA10GENIChomozygous108863521
17139664171396642GT9GENIChomozygous109104382
17139729571397296TC18GENIChomozygous108863524
17139797471397975GA13GENIChomozygous109104384
17139813071398131AC15GENIChomozygous108863527
17139853871398539CA17GENIChomozygous109104386
17139885671398857GA8GENIChomozygous109104388
17140022071400221CG13GENIChomozygous108863528
17140031171400312GA5GENIChomozygous108863529
17138526371385263GAGTGTGTGTGA16GENIChomozygous134387143
17139068871390688CA16GENIChomozygous134387144
17139069071390692TG17GENIChomozygous134387145
17139151771391532TCTTCAGACACACCA15GENIChomozygous134387146
17139859271398592A15GENIChomozygous134387147
17140074871400751GTC11GENIChomozygous134387148
17139353571393536GT12GENIChomozygous108131689