chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230368247230368248AG24GENIChomozygous60084989
2230368694230368695TA11GENIChomozygous62058787
2230368695230368696AC11GENIChomozygous62058788
2230369215230369216GA12GENIChomozygous62058789
2230370442230370443GT9GENIChomozygous60084994
2230370879230370880CT16GENIChomozygous59431830
2230371516230371517CT21GENIChomozygous62058790
2230376837230376838GA25GENICpossibly homozygous62058791
2230377018230377019TC21GENIChomozygous60084995
2230377655230377656GA9GENIChomozygous62058792
2230378780230378781TC20GENIChomozygous60084996
2230379060230379061A-16GENIChomozygous61678714
2230382465230382466TA20GENIChomozygous60084999
2230383135230383136TC11GENIChomozygous59431835
2230384374230384375CT19GENIChomozygous62058794
2230385989230385990CT7GENIChomozygous60085002
2230387370230387371TA15GENIChomozygous60085004
2230387465230387466C-16GENIChomozygous62058795
2230388651230388652AAT10GENIChomozygous61601885
2230389275230389276TC19GENIChomozygous62058796
2230391222230391223CG10GENIChomozygous62058797
2230391859230391860GC25GENIChomozygous60085006
2230391942230391943AG19GENIChomozygous62058798
2230392250230392251GA12GENIChomozygous62058799
2230392307230392308TTAGAC8GENIChomozygous62058801
2230392879230392880TG14GENIChomozygous62058802
2230394024230394025AG19GENIChomozygous59431844
2230394444230394445TC14GENIChomozygous59431845
2230394461230394462A-9GENIChomozygous62058803
2230396269230396271AG--12GENIChomozygous62058804
2230398591230398592AG20GENIChomozygous59431849
2230400552230400553AAT13GENIChomozygous60085017
2230401343230401346AAG---24GENIChomozygous62058805
2230401593230401594TC15GENIChomozygous62058806
2230402373230402374CA16GENIChomozygous62058807
2230403043230403044TA15GENIChomozygous62058808