chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172138542721385428AG9GENIChomozygous111298434
172138762921387630AG41GENIChomozygous110987562
172138882521388826AG37GENIChomozygous110987564
172138996821389969CT30GENIChomozygous110987568
172139041821390419CA36GENIChomozygous110987570
172139079721390798TC42GENIChomozygous110987572
172139133221391333TA23GENIChomozygous110987574
172139449621394497GT29GENIChomozygous111178017
172139476921394770CA15GENICpossibly homozygous110987578
172139477521394776CA4GENIChomozygous110987580
172139700721397008CG35GENIChomozygous110987582
172139951121399512CT34GENIChomozygous110987584
172139963821399639GA31GENIChomozygous110987586
172140472121404722GA35GENIChomozygous110987588
172140518221405183GC18GENIChomozygous110987590
172140636021406361TA42GENIChomozygous111413331
172140689921406900TG38GENIChomozygous110987594
172140824221408243AT31GENIChomozygous111413333
172140898521408986TG22GENIChomozygous110987596
172141049921410500AG37GENIChomozygous110987598
172141257121412572CT26GENIChomozygous111413335
172141963621419637CT41GENIChomozygous110987600
172141992421419925AG21GENIChomozygous110987602
172142009421420095GC26GENIChomozygous110987604
172142025721420258TC29GENIChomozygous110987606
172142027621420277CT34GENIChomozygous110987608
172142088521420886TA30GENIChomozygous110987610
172142201321422014AT11GENIChomozygous110987614