chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
19017837090178371GA29GENIChomozygous660987084
19017892590178926AG16GENIChomozygous660987085
19017991290179913A-17GENIChomozygous763647575
19018188090181881CT23GENIChomozygous660987086
19018190490181905AAT21GENICheterozygous763647578
19018190490181905AATT21GENICpossibly homozygous763647579
19018190490181905AATTT21GENICheterozygous763647580
19018445890184459TA27GENIChomozygous660987087
19018477490184775GC27GENIChomozygous660987088
19018758390187585CT--8GENIChomozygous763647582
19019042190190422TTA16GENICheterozygous763647584
19019042190190422TTAA16GENICheterozygous763647585
19019186690191867TTA11GENIChomozygous763647587
19019620390196204GGCACTGGT25GENIChomozygous763647588
19019620590196206AAAAC27GENIChomozygous763647589