chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101047975810479759GT12GENICheterozygous591647319
101048004410480045GC10GENIChomozygous589958549
101048036610480367GC11GENICpossibly homozygous589958550
101048130710481308GA12GENIChomozygous591647320
101048132310481324CA13GENIChomozygous591647321
101048151910481521TT--3GENICheterozygous723311918
101048437010484371GA12GENICpossibly homozygous591647322
101048679710486798CT13GENICpossibly homozygous591647323
101048729410487295GC16GENIChomozygous589958551
101048929310489294CT6GENICheterozygous591647324
101049118910491190GT18GENICpossibly homozygous589958552
101049179710491798TTA10GENIChomozygous723311920
101049886610498867AG10GENICpossibly homozygous589958553
101050028110500282TC3GENIChomozygous589958554
101050029410500295TG2GENICheterozygous589958555
101050176910501770TC13GENICpossibly homozygous589958556
101050317710503178GA17GENICpossibly homozygous589958557
101050330210503303GA7GENIChomozygous589958558
101050397710503978TG11GENIChomozygous589958559
101050718410507185AG5GENIChomozygous589958560
101051072210510723AG15GENIChomozygous589958561
101051149610511497AC17GENICpossibly homozygous589958562
101051191910511920TC3GENIChomozygous589958563