chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106473719864737199CA44GENIChomozygous116617849
106473759364737594TA59GENIChomozygous116617851
106473768964737690TC51GENIChomozygous116617853
106473823064738231TC67GENIChomozygous116617855
106474020564740206GT3GENIChomozygous116617857
106474107864741079AG24GENICpossibly homozygous116617859
106474132364741324GA58GENIChomozygous116617861
106474387264743873TG67GENIChomozygous116617863
106474759264747593CT58GENIChomozygous116617865
106475182064751821AG64GENIChomozygous116617867
106475622664756227AG55GENIChomozygous116617869
106475771564757716AG66GENICheterozygous118075125
106475774664757747TC71GENICheterozygous118075126
106475787964757880CT74GENICheterozygous118041441
106475803364758034TG55GENICheterozygous117998504
106475788264757886TTTG73GENICheterozygous131465848
106475803164758032TA56GENICheterozygous128870681
106475803264758033CA56GENICheterozygous128870682
106475810264758103CG57GENICheterozygous117998505
106475821164758212CT94GENICheterozygous117998506
106475806664758070TTCC51GENICheterozygous128824740