chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230368247230368248AG22GENIChomozygous60084989
2230368694230368695TA8GENIChomozygous62058787
2230368695230368696AC8GENIChomozygous62058788
2230369215230369216GA13GENIChomozygous62058789
2230369382230369383TC8GENIChomozygous60084991
2230370442230370443GT10GENIChomozygous60084994
2230370879230370880CT13GENIChomozygous59431830
2230371516230371517CT22GENIChomozygous62058790
2230376837230376838GA15GENIChomozygous62058791
2230377018230377019TC17GENIChomozygous60084995
2230377655230377656GA12GENIChomozygous62058792
2230378780230378781TC13GENIChomozygous60084996
2230382465230382466TA22GENIChomozygous60084999
2230383135230383136TC15GENIChomozygous59431835
2230383623230383627AAAT----9GENIChomozygous59431836
2230384374230384375CT19GENIChomozygous62058794
2230385989230385990CT18GENIChomozygous60085002
2230387465230387466C-18GENIChomozygous62058795
2230388651230388652AAT19GENIChomozygous61601885
2230389275230389276TC22GENICpossibly homozygous62058796
2230391222230391223CG15GENIChomozygous62058797
2230391859230391860GC18GENIChomozygous60085006
2230391942230391943AG15GENIChomozygous62058798
2230392250230392251GA16GENIChomozygous62058799
2230392275230392276TTAA8GENIChomozygous62058800
2230392307230392308TTAGAC11GENIChomozygous62058801
2230392879230392880TG15GENIChomozygous62058802
2230394024230394025AG13GENIChomozygous59431844
2230394444230394445TC13GENIChomozygous59431845
2230394461230394462A-8GENIChomozygous62058803
2230394867230394868A-9GENIChomozygous62009723
2230396269230396271AG--21GENIChomozygous62058804
2230398591230398592AG13GENIChomozygous59431849
2230400552230400553AAT13GENIChomozygous60085017
2230401343230401346AAG---8GENIChomozygous62058805
2230401593230401594TC17GENIChomozygous62058806
2230402373230402374CA17GENIChomozygous62058807
2230403043230403044TA13GENIChomozygous62058808
2230381438230381440AC--23GENICheterozygous62434548