chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101281551912815520TG36GENIChomozygous142216763
101281581812815819AG14GENIChomozygous142216764
101281600012816001TA25GENIChomozygous142216765
101281681412816815CG20GENIChomozygous142216766
101281705512817056GA24GENIChomozygous142216767
101281706512817066TC29GENIChomozygous142216768
101281838112818382AG44GENIChomozygous142216769
101281861512818616TA23GENIChomozygous142216770
101281874712818748GA26GENIChomozygous142216771
101281923912819240AG15GENIChomozygous142216772
101281946212819463AC38GENIChomozygous142216773
101281971612819717TC28GENIChomozygous142216774
101282030212820303AG26GENIChomozygous142216775
101282064112820642GT18GENIChomozygous142216776
101282163612821637TA16GENIChomozygous142216777
101282179112821792CT26GENIChomozygous142216778
101282204412822045CT31GENIChomozygous142216779
101282208012822081AG33GENIChomozygous142216780
101282209712822098CT33GENIChomozygous142216781
101282963112829632AC27GENIChomozygous142216782
101283257012832571AC38GENIChomozygous142216783
101283322912833230CT26GENIChomozygous142216784
101283467812834679TC31GENIChomozygous142216785
101283506712835068TA21GENIChomozygous142216786
101283562612835627CT39GENIChomozygous142216787
101283564912835650AT32GENIChomozygous154677666
101283782212837823TC32GENIChomozygous142216788
101284059212840593AG26GENIChomozygous142216789
101284656512846566CT29GENIChomozygous142216790
101284789212847893AG27GENIChomozygous142216791
101283564912835650A32GENICheterozygous403276641
101284656512846566CA29GENICheterozygous403276642
101282133512821336T26GENIChomozygous142196519
101284843812848439G22GENIChomozygous142196520