chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148031426980314270CT24GENIChomozygous113500616
148031562980315630TC13GENIChomozygous113500617
148031647780316478GA23GENIChomozygous113500618
148031697580316976GA16GENIChomozygous113500619
148031785080317851CT14GENIChomozygous113500620
148031787080317871TC14GENIChomozygous113500621
148031881980318820GA15GENIChomozygous113500622
148031900780319008AG14GENIChomozygous113500623
148032007880320079AG16GENIChomozygous113500624
148032169080321691CT13GENIChomozygous113500625
148032222880322229AG14GENICpossibly homozygous113500626
148032386280323863AT23GENIChomozygous113500627
148033135180331352CT34GENIChomozygous113500628
148033135280331353AG34GENIChomozygous113500629
148033228880332289TG22GENIChomozygous113500630
148033477880334779TA27GENIChomozygous113500631
148033509480335095GA19GENIChomozygous113500632
148033748080337481CG13GENIChomozygous113500633
148034107780341078AG23GENIChomozygous113500634
148034127980341280GA28GENIChomozygous113500635
148034170980341710TC6GENIChomozygous113500636
148035220280352203TC30GENIChomozygous113500637
148035317580353176TC20GENIChomozygous113500638
148035411880354119TC5GENICheterozygous114098158
148035787380357874CT21GENIChomozygous113500639