chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105662624356626244AG18GENIChomozygous116783730
105662727356627274AC2GENIChomozygous117059792
105662805956628060AG23GENIChomozygous116783732
105662911856629119CT34GENIChomozygous116783734
105662938856629389TC29GENIChomozygous116783736
105662978456629785CT27GENIChomozygous116783738
105663148556631486CT27GENIChomozygous117011566
105663248056632481CA21GENIChomozygous116783742
105663374856633749CT26GENIChomozygous116783744
105663380256633803CT28GENIChomozygous116783746
105663395756633958AG30GENIChomozygous116783748
105663436856634369AT22GENIChomozygous116783750
105663467556634676GA22GENIChomozygous116783752
105663468256634683TG21GENIChomozygous116783754
105663494456634945GT16GENIChomozygous116783756
105663704356637044CG25GENIChomozygous117059796
105663929356639294AG31GENIChomozygous116783760
105664022856640229AG18GENIChomozygous116783762
105664038656640387TC26GENIChomozygous116783764
105664074156640742TC32GENIChomozygous116783766
105664218456642185CT17GENIChomozygous117078894
105664284156642842AG24GENIChomozygous116783768
105664451056644511TG27GENIChomozygous116783772
105664506356645064CT25GENIChomozygous117059798
105664571556645716TA24GENIChomozygous116783774
105664659456646595TC19GENIChomozygous116783778
105664698156646982AT20GENIChomozygous116783780
105664751956647520TC22GENIChomozygous116783782
105664970056649701CT21GENIChomozygous117059800
105665085856650859AG26GENIChomozygous117059802
105665115956651160CT20GENIChomozygous117059804
105665138356651384TC17GENIChomozygous116783788
105665156056651561CT12GENIChomozygous117059806
105665217656652177GA33GENIChomozygous117059808