chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101808104818081049GGT20GENICpossibly homozygous51335556
101808110118081105TTTT----9GENICpossibly homozygous51335557
101808145718081458TC27GENIChomozygous51335558
101808193818081939CT14GENIChomozygous51628938
101808308918083090GA15GENIChomozygous51628939
101808367718083678GA12GENIChomozygous51335561
101808491918084920CCACAG15GENIChomozygous51335564
101808580018085801GA10GENIChomozygous51335565
101808582818085829TC14GENIChomozygous51335566
101808589018085891TC20GENIChomozygous51335567
101808667618086677TA17GENIChomozygous51335569
101808668218086683TTTGAC18GENIChomozygous51335570
101808726318087267TTTT----1GENIChomozygous51335571
101808822418088225AC14GENIChomozygous51335572
101809072018090721GT27GENIChomozygous51335574
101809078018090781AG30GENIChomozygous51335575
101809085318090854AG30GENIChomozygous51628940
101808472618084727TTCTCACACAAAAGCAAGGGTGCCACCA35GENIChomozygous52358082
101808560818085616TCTCTCTT--------2GENICheterozygous52358084
101809013618090137CCA2GENICheterozygous52358086
101809025918090260GGTTTTTTTTTTTTTTTTGTCTAAAATATTTTTTTTTTATTAACTTGAGTATTTC7GENICheterozygous52358088
101808593318085934CT17GENIChomozygous51815733
101808879118088792GA20GENIChomozygous51815735