chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
19017837090178371GA29GENIChomozygous61461575
19017892590178926AG16GENIChomozygous61461577
19017991290179913A-17GENIChomozygous62350008
19018188090181881CT23GENIChomozygous62534800
19018190490181905AATTT21GENICheterozygous61461585
19018190490181905AATT21GENICpossibly homozygous61461587
19018190490181905AAT21GENICheterozygous62140310
19018445890184459TA27GENIChomozygous61461589
19018477490184775GC27GENIChomozygous61461591
19018758390187585CT--8GENIChomozygous62140313
19019042190190422TTA16GENICheterozygous61461596
19019042190190422TTAA16GENICheterozygous62140315
19019186690191867TTA11GENIChomozygous61298415
19019620390196204GGCACTGGT25GENIChomozygous61461598
19019620590196206AAAAC27GENIChomozygous61461600