chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
995820299582030CCA8GENICheterozygous771245425
995846439584644CT25GENICpossibly homozygous675208585
995854599585460C-22GENIChomozygous771245426
995863329586333GA33GENICpossibly homozygous675208586
995866859586686TC13GENIChomozygous675208587
995881049588105CT16GENICheterozygous675208588
995884459588446CT33GENICpossibly homozygous675208589
995887389588746GTGCATAG--------33GENICpossibly homozygous771245428
995914299591430CT30GENICpossibly homozygous675208590
995942079594208GGT22GENIChomozygous771245429
995996489599649TA31GENICpossibly homozygous675208591
996030959603096GA19GENIChomozygous675208592
996036099603610TC34GENIChomozygous675208593
996076249607625GGA7GENICheterozygous771245431
996099349609938CAGA----14GENIChomozygous771245432
996135579613558TTC14GENIChomozygous771245433
996143339614334GGTC2GENIChomozygous771245435
996149809614981TTTTTG22GENICpossibly homozygous771245436
996150059615006CT30GENIChomozygous675208594
996153869615387AT35GENIChomozygous675208595
996173039617304A-1GENIChomozygous771245437
996195799619580CCCA29GENIChomozygous771245438
996195829619583G-31GENIChomozygous771245439
996195849619585TTCA31GENIChomozygous771245440
996195859619586GC30GENIChomozygous675208596
996251939625194TG28GENIChomozygous675208597
996252419625243TT--11GENICheterozygous771245442
996252429625243T-11GENICheterozygous771245443
996268099626810AC12GENIChomozygous675208598
996269829626989GCCCCGG-------2GENIChomozygous771245444
996270239627024AAGTCTCG9GENIChomozygous771245445
996307999630800TTCA14GENICheterozygous771245447
996307999630800TTCACACACA14GENICheterozygous771245448
996308009630802CA--14GENICheterozygous771245446
996327209632721AG23GENIChomozygous675208599
996340849634085CCACAA4GENIChomozygous771245450
996356559635657GT--2GENIChomozygous771245452
996372449637245CA30GENIChomozygous675208600