chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31735694917356950CT26GENIChomozygous57176637
31735728117357282TC27GENIChomozygous57176639
31735764517357646TC35GENIChomozygous57176641
31735764617357647GA35GENIChomozygous57176643
31735769517357696GA36GENIChomozygous57176645
31735777017357771CT38GENIChomozygous57176647
31735791717357918CT38GENIChomozygous57176649
31735791817357919AG38GENIChomozygous57176651
31735793317357934TC35GENIChomozygous57176653
31735795917357960TC33GENIChomozygous57176655
31735799617357997AG30GENIChomozygous57176657
31735822617358227CA30GENIChomozygous57176659
31735825417358255GA34GENIChomozygous57176661
31735827317358274GA33GENIChomozygous57176663
31735839717358398CT44GENICpossibly homozygous57176665
31735851217358513TC25GENIChomozygous57176667
31735856617358567TC29GENIChomozygous57176669
31735962417359625GA24GENIChomozygous57176671
31735963517359636GA24GENIChomozygous57176673
31736033617360337GA21GENIChomozygous57176675
31736163217361633CT25GENIChomozygous57176683
31736173517361736GT3GENIChomozygous57176685
31736177717361778TA1GENIChomozygous57176687
31736190617361907CT17GENIChomozygous57176689
31736217717362178TG15GENIChomozygous57176691
31736226917362270CT25GENIChomozygous57176693
31736268017362681AG34GENIChomozygous57176695
31736300617363016ACCAGCCCCG----------19GENIChomozygous57176697
31736315317363154AG13GENIChomozygous57176699
31736315517363156AAGGG12GENIChomozygous57176701
31736330717363308TG25GENIChomozygous57176703
31736428117364282TG27GENIChomozygous57176705
31736512717365128GA15GENIChomozygous57176707