chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175079202550792026CT20GENIChomozygous47127873
175079206850792069GC23GENIChomozygous47127874
175079220550792206CG29GENIChomozygous47127875
175079260250792603GA35GENIChomozygous47127876
175079281050792811AG55GENIChomozygous47127877
175079289550792896AG57GENIChomozygous47127878
175079310250793103TTA15GENICpossibly homozygous47127879
175079315150793152AC25GENIChomozygous47127880
175079318450793185AG24GENIChomozygous47127881
175079326350793264T-33GENIChomozygous47127882
175079331450793315TC34GENIChomozygous47127883
175079332850793329CT33GENIChomozygous47127884
175079337850793379CT36GENIChomozygous47127885
175079341450793415AG38GENIChomozygous47127886
175079369550793696CT23GENICpossibly homozygous47127887
175079369650793697GA23GENIChomozygous47127888
175079393650793937AC17GENIChomozygous47127889
175079452150794522GC17GENICheterozygous47127890
175079452850794529GA18GENICheterozygous47127891
175079453750794538CT21GENICpossibly homozygous47127892
175079455650794557GA25GENICheterozygous47127893
175079459550794596CT26GENICheterozygous47127894
175079467750794678T-16GENIChomozygous47127895
175079467750794678TTA12GENIChomozygous47127896
175079469050794691TA17GENIChomozygous47127899
175079467850794679TA19GENICheterozygous47127897
175079468650794687TA17GENIChomozygous47127898
175079505850795059GA47GENIChomozygous47127900
175079520050795201TC44GENIChomozygous47127901
175079567650795677CT48GENICpossibly homozygous47127902
175079672750796728GA34GENIChomozygous47127903
175079678550796786CT27GENIChomozygous47127904
175079713550797136TC31GENIChomozygous47127905
175079759550797596CT45GENIChomozygous47127906
175079842150798422TTGC33GENICpossibly homozygous47127907
175079842650798427AG36GENICheterozygous47127908
175079844450798445AT30GENICpossibly homozygous47127909
175079844450798445AACT19GENICpossibly homozygous47127910
175079852150798522CT33GENIChomozygous47127911
175080012550800126AG52GENICpossibly homozygous47127912