chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101281551912815520TG58GENICpossibly homozygous142216763
101281581812815819AG47GENIChomozygous142216764
101281600012816001TA48GENIChomozygous142216765
101281681412816815CG48GENIChomozygous142216766
101281705512817056GA38GENIChomozygous142216767
101281706512817066TC37GENIChomozygous142216768
101281838112818382AG60GENIChomozygous142216769
101281861512818616TA37GENICpossibly homozygous142216770
101281874712818748GA50GENIChomozygous142216771
101281923912819240AG69GENIChomozygous142216772
101281946212819463AC57GENICpossibly homozygous142216773
101281971612819717TC60GENIChomozygous142216774
101282030212820303AG42GENIChomozygous142216775
101282064112820642GT37GENIChomozygous142216776
101282133512821336T39GENIChomozygous142196519
101282163612821637TA35GENIChomozygous142216777
101282179112821792CT42GENIChomozygous142216778
101282204412822045CT62GENIChomozygous142216779
101282208012822081AG63GENIChomozygous142216780
101282209712822098CT61GENIChomozygous142216781
101282963112829632AC44GENIChomozygous142216782
101283257012832571AC65GENICpossibly homozygous142216783
101283322912833230CT51GENIChomozygous142216784
101283467812834679TC76GENIChomozygous142216785
101283506712835068TA52GENIChomozygous142216786
101283562612835627CT52GENIChomozygous142216787
101283782212837823TC70GENIChomozygous142216788
101284059212840593AG43GENIChomozygous142216789
101284656512846566CT45GENIChomozygous142216790
101284789212847893AG65GENIChomozygous142216791
101284843812848439G54GENIChomozygous142196520
101283564912835650A40GENICheterozygous403276641
101283564912835650AT40GENIChomozygous154677666
101284656512846566CA45GENICheterozygous403276642