chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101808104818081049GGT19GENICpossibly homozygous51335556
101808110118081105TTTT----11GENIChomozygous51335557
101808145718081458TC23GENIChomozygous51335558
101808193818081939CT18GENIChomozygous51628938
101808308918083090GA27GENIChomozygous51628939
101808367718083678GA17GENIChomozygous51335561
101808472618084727TTCTCACACAAAAGCAAGGGTGCCACCA22GENIChomozygous52358082
101808491918084920CCACAG13GENIChomozygous51335564
101808560818085616TCTCTCTT--------3GENIChomozygous52358084
101808580018085801GA8GENIChomozygous51335565
101808582818085829TC11GENIChomozygous51335566
101808589018085891TC21GENIChomozygous51335567
101808667618086677TA22GENIChomozygous51335569
101808668218086683TTTGAC22GENIChomozygous51335570
101808726318087267TTTT----7GENIChomozygous51335571
101808822418088225AC20GENIChomozygous51335572
101809013618090137CCA6GENIChomozygous52358086
101809025918090260GGTTTTTTTTTTTTTTTTGTCTAAAATATTTTTTTTTTATTAACTTGAGTATTTC6GENICheterozygous52358088
101809072018090721GT38GENIChomozygous51335574
101809078018090781AG31GENIChomozygous51335575
101809085318090854AG39GENIChomozygous51628940
101808879118088792GA22GENIChomozygous51815735
101808593318085934CT21GENIChomozygous51815733