chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167394907073949071GA31GENIChomozygous64584787
167395067573950676CT42GENIChomozygous64584790
167395345973953460CT29GENICheterozygous64584796
167395558073955581AG51GENIChomozygous64584805
167395811973958120AG48GENIChomozygous64584808
167395874873958749AG43GENIChomozygous64584811
167396168673961687AG32GENIChomozygous64584813
167396199273961993GA26GENIChomozygous64584816
167396351673963517TC50GENIChomozygous64584819
167396371873963719AG42GENIChomozygous64584822
167396424373964244AT21GENICpossibly homozygous64584825
167396446473964465CT19GENIChomozygous64584828
167396763773967638CT42GENIChomozygous64584837
167396890173968902AG28GENIChomozygous64584840
167416712374167124CT37GENIChomozygous64584845
167416790174167902GA42GENIChomozygous64584848
167416866574168666CT28GENIChomozygous64584851
167416880474168805CT55GENIChomozygous64584854
167416952874169529CA45GENIChomozygous64584857
167416971874169719TG20GENIChomozygous64584860
167417053074170531AC46GENIChomozygous64584863
167417120974171210AG18GENIChomozygous64584867
167417155774171558TA22GENIChomozygous64584869
167417272374172724TG18GENIChomozygous64584872
167417310074173101TA21GENIChomozygous64584875
167417396474173965CT39GENIChomozygous64584878
167417415674174157CT5GENIChomozygous64584881