chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
665627326562733CT62GENIChomozygous141800713
665679026567903TC73GENIChomozygous141800714
665688716568872C46GENIChomozygous141773969
665688796568880AG50GENIChomozygous141800715
665702296570230GA63GENIChomozygous141800716
665703736570373A50GENICpossibly homozygous141773970
665706146570689TGGGGCTGGAGCGATGGCTCAGAGGTTAAGAGCACTGTCTGCTCTTCCAGAGTTCAATTCCCAGCAACCACATGG38GENIChomozygous141773971
665713646571364A41GENICpossibly homozygous141773972
665717536571753AGG50GENIChomozygous141773973
665717646571764TCCA51GENIChomozygous141773974
665730846573085GC68GENICpossibly homozygous141800717
665732596573260TA59GENIChomozygous141800718
665733566573357TC67GENIChomozygous141800719
665735606573561CA51GENIChomozygous141800720
665735626573563TG52GENIChomozygous141800721
665735666573567TG50GENIChomozygous141800722
665735766573577CA47GENIChomozygous141800723
665735826573583TA45GENIChomozygous141800724
665735866573587GA47GENIChomozygous141800725
665735916573591CA50GENIChomozygous141773975
665736326573633AG59GENIChomozygous141800726
665739606573961GA63GENIChomozygous141800727
665750106575013CTC70GENIChomozygous141773976
665754196575420TC56GENIChomozygous141800728
665759486575949TC54GENICpossibly homozygous141800729
665766676576668TC76GENIChomozygous141800730
665784216578422TC33GENIChomozygous141800731
665784236578424TC31GENIChomozygous141800732
665784196578420TC25GENICheterozygous144751806