chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101281551912815520TG17GENIChomozygous142216763
101281581812815819AG17GENIChomozygous142216764
101281600012816001TA13GENIChomozygous142216765
101281681412816815CG14GENIChomozygous142216766
101281705512817056GA19GENIChomozygous142216767
101281706512817066TC20GENIChomozygous142216768
101281838112818382AG25GENIChomozygous142216769
101281861512818616TA13GENIChomozygous142216770
101281874712818748GA16GENIChomozygous142216771
101281923912819240AG20GENIChomozygous142216772
101281946212819463AC25GENIChomozygous142216773
101281971612819717TC17GENIChomozygous142216774
101282030212820303AG8GENIChomozygous142216775
101282064112820642GT18GENIChomozygous142216776
101282163612821637TA9GENIChomozygous142216777
101282179112821792CT16GENIChomozygous142216778
101282204412822045CT17GENIChomozygous142216779
101282208012822081AG16GENIChomozygous142216780
101282209712822098CT14GENIChomozygous142216781
101282963112829632AC19GENIChomozygous142216782
101283257012832571AC25GENIChomozygous142216783
101283322912833230CT15GENIChomozygous142216784
101283467812834679TC16GENIChomozygous142216785
101283506712835068TA16GENIChomozygous142216786
101283562612835627CT13GENIChomozygous142216787
101283564912835650AT8GENIChomozygous154677666
101283782212837823TC18GENIChomozygous142216788
101284059212840593AG16GENIChomozygous142216789
101284656512846566CT16GENIChomozygous142216790
101284789212847893AG24GENIChomozygous142216791
101283564912835650A8GENICheterozygous403276641
101284656512846566CA16GENICheterozygous403276642
101284843812848439G13GENIChomozygous142196520
101282133512821336T18GENIChomozygous142196519