chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12300587123005872AG18GENIChomozygous61273480
12300648123006482AG27GENIChomozygous61273481
12300663923006640AC18GENIChomozygous62526746
12300664023006641GT19GENIChomozygous62526747
12300854323008546GTG---3GENICheterozygous60639078
12300865423008655GGACACAGACACAGAC5GENIChomozygous62121525
12300891323008917AGAG----6GENIChomozygous62121526
12300947923009481TT--20GENIChomozygous61273485
12300988023009881AT31GENIChomozygous62526748
12300995123009952GA29GENIChomozygous62526749
12301010323010104GA28GENIChomozygous61273487
12301046723010468GT16GENIChomozygous61395140
12301081723010818AG25GENIChomozygous62526750
12301106923011070AG21GENIChomozygous61273489
12301122323011224TG19GENIChomozygous61273490
12301125423011255GC16GENIChomozygous61273491
12301130323011304AG7GENIChomozygous61273492
12301136823011369AG2GENIChomozygous61273493
12301137923011380A-4GENIChomozygous62072643
12301138023011381AG3GENIChomozygous62072645
12301176223011763TC20GENIChomozygous61273495
12301178123011782CG23GENIChomozygous61273496
12301178523011786GA23GENIChomozygous61273497
12301202023012021TC42GENIChomozygous61273498
12301260023012601C-20GENIChomozygous62541345
12301284823012849AG16GENIChomozygous62526751
12301293323012937AAAA----20GENIChomozygous61273502
12301306723013068T-25GENIChomozygous61273503
12301335423013358AGGA----23GENIChomozygous62541346
12301336023013364GATA----22GENIChomozygous62541347
12301336823013371CAT---20GENIChomozygous62541348
12301348323013484TC25GENIChomozygous62526752
12301349823013499TC23GENIChomozygous61273504
12301536123015373TGTGTGTGTGTG------------7GENICpossibly homozygous62541349
12301542823015429CT19GENIChomozygous62716720
12301619723016198GGTA12GENIChomozygous61395155
12301624223016243AATAATGTT21GENIChomozygous61395157
12301635923016360GA21GENIChomozygous61981265