chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141058339141058340CCAG36GENIChomozygous55753822
5141058762141058763GGA10GENIChomozygous55753823
5141058778141058779GGA18GENIChomozygous55753824
5141058812141058813GA30GENIChomozygous55753825
5141059467141059468GA28GENIChomozygous55753826
5141062649141062650TTGG41GENIChomozygous55753827
5141063526141063527AT34GENIChomozygous55753828
5141063618141063620AA--11GENIChomozygous55753829
5141063765141063766AG21GENIChomozygous55753830
5141066515141066516GT29GENIChomozygous55753831
5141068528141068529TTAATA7GENICpossibly homozygous55753832
5141069921141069922GT30GENIChomozygous55753833
5141070769141070770CT24GENIChomozygous55753834