chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14384991843849919AG20GENICheterozygous60694499
14385971143859713TG--13GENICheterozygous60694500
14386548343865484GT33GENICheterozygous60694501
14388113643881137TC39GENIChomozygous60694502
14388120343881204TTC21GENIChomozygous60694503
14388120543881206GC20GENIChomozygous60694504
14388120743881208GA21GENIChomozygous60694505
14388121243881213A-17GENICpossibly homozygous60694506
14391187543911876TTAC8GENICpossibly homozygous60694507
14391202543912026GT11GENIChomozygous60694508
14391203743912038AT8GENIChomozygous60694509
14391204643912047GGT10GENIChomozygous60694510
14391207743912078C-7GENIChomozygous60694511
14391207943912080C-6GENIChomozygous60694512
14391208943912090C-8GENIChomozygous60694513
14391209543912096A-8GENIChomozygous60694514
14391824843918249A-11GENIChomozygous60694515