chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141058339141058340CCAG54GENIChomozygous55753822
5141058762141058763GGA26GENICpossibly homozygous55753823
5141058778141058779GGA29GENIChomozygous55753824
5141058812141058813GA36GENIChomozygous55753825
5141059467141059468GA55GENIChomozygous55753826
5141062649141062650TTGG44GENIChomozygous55753827
5141063526141063527AT67GENIChomozygous55753828
5141063618141063620AA--2GENIChomozygous55753829
5141063765141063766AG47GENIChomozygous55753830
5141066515141066516GT38GENIChomozygous55753831
5141068528141068529TTAATA3GENIChomozygous55753832
5141069921141069922GT54GENICpossibly homozygous55753833
5141070769141070770CT31GENIChomozygous55753834