chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104695639346956394CT41GENICpossibly homozygous116586909
104696106246961063GA53GENIChomozygous116586911
104696111446961115GT47GENIChomozygous116586913
104696236646962367TC43GENIChomozygous116586915
104696396246963963TA48GENIChomozygous116586917
104696401246964013TC44GENIChomozygous116586919
104696417146964172GA55GENIChomozygous116586921
104696459446964595GT65GENICheterozygous117253079
104696477946964780CT31GENIChomozygous116586923
104696539946965400TC35GENIChomozygous116586925
104696606046966061AG28GENIChomozygous116773062
104696620046966201GT23GENIChomozygous116586927
104696671246966713GA29GENIChomozygous116586931
104696714446967145AG33GENIChomozygous116586933
104696729746967298AG21GENIChomozygous116586935
104696730846967309CT24GENIChomozygous116586937
104696783546967836CT32GENIChomozygous116586939
104696822646968227TC40GENIChomozygous116586941
104696861246968613TC32GENIChomozygous116586943
104696889146968892TG49GENIChomozygous116586945