chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1743006564300657AC5GENIChomozygous791566439
1743008454300846GT10GENIChomozygous791566440
1743074354307436GA29GENICheterozygous791566441
1743074504307451AT34GENICheterozygous791566442
1743074584307459AG40GENICheterozygous791566443
1743075314307532AT98GENICheterozygous791566444
1743075334307534GT97GENICheterozygous791566445
1743076394307640AC40GENICheterozygous791566446
1743077414307742TC63GENICheterozygous791566447
1743346924334693GA17GENIChomozygous791566448
1743718914371892GA29GENICheterozygous791566449
1743911014391102GA21GENIChomozygous791566450
1743911614391162CG17GENIChomozygous791566451
1743912194391220GA16GENIChomozygous791566452
1743912324391233GA12GENICpossibly homozygous791566453
1743912544391255CT9GENIChomozygous791566454
1743912584391259GA9GENIChomozygous791566455
1743912704391271GT13GENIChomozygous791566456
1743912764391277CA13GENIChomozygous791566457
1744109024410903CT43GENICheterozygous791566458
1744109044410905GC42GENICheterozygous791566459
1744109454410946AG39GENICheterozygous791566460
1744109484410949AG38GENICheterozygous791566461
1744109974410998AG20GENICheterozygous791566462
1744110004411001AG18GENICheterozygous791566463
1744110164411017AG23GENICheterozygous791566464