chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7135839031135839032GA56GENICheterozygous116092203
7135839116135839117TC35GENIChomozygous115920622
7135839117135839118GA35GENICheterozygous116092205
7135839779135839780TA3GENIChomozygous115920624
7135840186135840187GA24GENIChomozygous115920628
7135841136135841137CT21GENIChomozygous115920630
7135841142135841143CT13GENIChomozygous115920632
7135841167135841168CT24GENIChomozygous115920634
7135841216135841217CG39GENIChomozygous115920636
7135841238135841239CT38GENIChomozygous115920638
7135841492135841493CT20GENIChomozygous115920640
7135842079135842080GA24GENIChomozygous115920642
7135842611135842612CT27GENIChomozygous115920644
7135842997135842998GA8GENIChomozygous115920646
7135843051135843052GT10GENIChomozygous115920648
7135843715135843716TC24GENIChomozygous115920650
7135844589135844590CT22GENIChomozygous115920652
7135844630135844631TC32GENIChomozygous115920654
7135846328135846329TA14GENIChomozygous115920656
7135847629135847630TC25GENIChomozygous115920658
7135848664135848665CT4GENIChomozygous115920660
7135849410135849411TG19GENIChomozygous115920662
7135849614135849615CT28GENIChomozygous115920664