chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101281551912815520TG54GENIChomozygous142216763
101281581812815819AG57GENIChomozygous142216764
101281600012816001TA40GENIChomozygous142216765
101281681412816815CG51GENIChomozygous142216766
101281705512817056GA57GENIChomozygous142216767
101281706512817066TC58GENIChomozygous142216768
101281838112818382AG71GENIChomozygous142216769
101281861512818616TA53GENIChomozygous142216770
101281874712818748GA65GENIChomozygous142216771
101281923912819240AG51GENIChomozygous142216772
101281946212819463AC54GENICpossibly homozygous142216773
101281971612819717TC52GENIChomozygous142216774
101282030212820303AG31GENIChomozygous142216775
101282064112820642GT29GENICpossibly homozygous142216776
101282163612821637TA25GENIChomozygous142216777
101282179112821792CT47GENIChomozygous142216778
101282204412822045CT59GENIChomozygous142216779
101282208012822081AG61GENIChomozygous142216780
101282209712822098CT59GENIChomozygous142216781
101282963112829632AC68GENIChomozygous142216782
101283257012832571AC76GENIChomozygous142216783
101283322912833230CT56GENIChomozygous142216784
101283467812834679TC57GENIChomozygous142216785
101283506712835068TA63GENIChomozygous142216786
101283562612835627CT56GENIChomozygous142216787
101283782212837823TC71GENIChomozygous142216788
101284059212840593AG41GENIChomozygous142216789
101284656512846566CT48GENIChomozygous142216790
101284789212847893AG63GENIChomozygous142216791
101281676412816765TA48GENICpossibly homozygous147575727
101283564912835650AT56GENIChomozygous154677666
101283564912835650A56GENICheterozygous403276641
101284656512846566CA48GENICheterozygous403276642
101282133512821336T24GENIChomozygous142196519
101284843812848439G54GENIChomozygous142196520