chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175079202550792026CT28GENIChomozygous554394700
175079206850792069GC25GENIChomozygous554394701
175079220550792206CG23GENIChomozygous554394702
175079260250792603GA33GENIChomozygous554394703
175079281050792811AG31GENIChomozygous554394704
175079289550792896AG28GENIChomozygous554394705
175079310250793103TTA17GENICpossibly homozygous702105089
175079315150793152AC24GENIChomozygous554394706
175079318450793185AG24GENIChomozygous554394707
175079326350793264T-21GENIChomozygous702105090
175079331450793315TC30GENIChomozygous554394708
175079332850793329CT27GENICpossibly homozygous554394709
175079337850793379CT23GENIChomozygous554394710
175079341450793415AG26GENIChomozygous554394711
175079369550793696CT36GENIChomozygous554394712
175079369650793697GA36GENIChomozygous554394713
175079393650793937AC23GENIChomozygous554394714
175079396450793965AT23GENIChomozygous554394715
175079447650794477CT24GENIChomozygous554394716
175079452150794522GC18GENIChomozygous554394717
175079452850794529GA18GENIChomozygous554394718
175079453750794538CT17GENIChomozygous554394719
175079455650794557GA18GENIChomozygous554394720
175079467750794678TTA5GENIChomozygous702105091
175079467850794679TA5GENIChomozygous554394721
175079505850795059GA15GENIChomozygous554394722
175079520050795201TC18GENIChomozygous554394723
175079567650795677CT38GENIChomozygous554394724
175079672750796728GA29GENIChomozygous554394725
175079678550796786CT22GENIChomozygous554394726
175079713550797136TC38GENIChomozygous554597242
175079759550797596CT29GENIChomozygous554394727
175079812050798121T-32GENIChomozygous702105092
175079827350798274GA38GENIChomozygous554394728
175079842150798422TTGC19GENIChomozygous702105093
175079852150798522CT37GENIChomozygous554394729
175080012550800126AG30GENIChomozygous554394730