chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91539452515394526GA40GENIChomozygous117267718
91539529215395293AG53GENIChomozygous117267719
91539560815395609CT60GENIChomozygous117267720
91539585515395856CT64GENIChomozygous117267721
91539605315396054CT54GENIChomozygous117267722
91539718515397185TTTTTTCTTTTTTCTTTTTTC20GENICheterozygous131697534
91539718615397186TTTTTCTTTTTTCTTTTTTC20GENICheterozygous128683316
91539792915397930TG49GENIChomozygous117267723
91539822915398230TC64GENIChomozygous117267724
91539834715398348GT46GENIChomozygous117267725
91539900115399002CT49GENIChomozygous117267726
91539902815399029AC52GENIChomozygous117267727
91539984515399846CT57GENIChomozygous117267728
91539985015399851AG56GENIChomozygous117267729
91539998715399988GT36GENICpossibly homozygous117267730
91540001515400016CG43GENIChomozygous117267731
91540039315400394AG61GENIChomozygous117267732
91540051915400520GA50GENIChomozygous117267733
91540062515400626CT49GENIChomozygous117267734
91540076915400770AG40GENIChomozygous117267735
91540086215400863GA50GENIChomozygous117267736
91540095815400959AG55GENIChomozygous117267737
91540102015401021CT62GENIChomozygous117267738
91540131515401316CT55GENIChomozygous117267739
91540142215401423TC50GENICpossibly homozygous117267740
91540149315401494TA43GENIChomozygous117267741
91540235215402353CT63GENIChomozygous117267742
91540246415402465AG55GENIChomozygous117267743
91540249615402496GCATGGAAG51GENIChomozygous128683317
91540253115402532TC59GENIChomozygous117267744
91540271315402714GA56GENIChomozygous117267745