chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28691004086910041GT19GENICheterozygous110949980
28691056786910568AG68GENICpossibly homozygous110949982
28691093486910935AG29GENIChomozygous110949984
28691109786911098AG13GENIChomozygous110949986
28691136286911363AG46GENIChomozygous110949988
28691136486911365CT48GENIChomozygous110949990
28691145886911459TC55GENICpossibly homozygous110949992
28691148086911481CT58GENIChomozygous110949994
28691167586911676AG54GENIChomozygous110949996
28691184186911842CG41GENIChomozygous110949998
28691190786911908GA59GENICpossibly homozygous110950000
28691200086912001CT32GENIChomozygous110950002
28691223186912232TC56GENICpossibly homozygous110950004
28691243386912434GA63GENIChomozygous110950006
28691255686912557AG70GENICpossibly homozygous110950008
28691255786912558AC70GENICpossibly homozygous110950010