chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108625769086257691CG20GENIChomozygous138842198
108625769286257693CA22GENIChomozygous138842199
108625774186257742AG20GENIChomozygous144416512
108625941986259420TC22GENIChomozygous144416513
108625963586259636GA14GENIChomozygous144416514
108625964686259647GC16GENIChomozygous144416515
108625964686259647GA16GENICheterozygous403293747
108626051886260519CA12GENICpossibly homozygous144416516
108626053686260537AT18GENIChomozygous144416517
108626062386260624AG22GENIChomozygous144416518
108626089586260901AACAAC10GENIChomozygous144412402
108625977586259778TTG23GENIChomozygous141119169
108625892186258921T17GENIChomozygous144412398
108625897286258972TTTTCTTTTT10GENIChomozygous144412399
108625951886259518CTTTA23GENIChomozygous144412400
108626004486260044TT21GENIChomozygous144412401
108626116186261162AT16GENIChomozygous144416519
108626143286261433TC27GENIChomozygous144416520
108626164686261647GA18GENIChomozygous144416521
108626164986261650CT16GENIChomozygous144416522
108626230886262309AG21GENIChomozygous144416523
108626288086262881AC17GENIChomozygous144416524
108626302086263021TC24GENIChomozygous144416525
108626303386263033TG24GENIChomozygous144412403
108626319286263193GA6GENIChomozygous144416526
108626324686263247GA10GENIChomozygous144416527
108626409486264095TG20GENIChomozygous144416528
108626458386264584AG15GENIChomozygous144416529
108626461686264617AG10GENIChomozygous144416530
108626475686264757GA19GENIChomozygous144416531
108626488286264884TG13GENIChomozygous144412404
108626491186264913AT17GENIChomozygous144412405
108626504886265049AG17GENIChomozygous144416532