chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227119041227119042TC18GENIChomozygous142867793
1227119350227119351AG15GENIChomozygous142867794
1227119786227119787TG19GENIChomozygous142867795
1227120305227120306AT19GENIChomozygous142867796
1227120330227120330A23GENIChomozygous135463383
1227120345227120346TC24GENIChomozygous142867797
1227120365227120365TGTAAGACT26GENIChomozygous142795399
1227120947227120948GT22GENIChomozygous142867798
1227121075227121076GT18GENIChomozygous142867799
1227121172227121172AGAAAAGATACTCA13GENIChomozygous142795400
1227121278227121279AC14GENIChomozygous142867800
1227121367227121368GA19GENIChomozygous142867801
1227121518227121519AG7GENIChomozygous142867802
1227122132227122132GGGGTGTGTGTGTGTATGAGGGGTGTGTGTGTGTATGAGGGGTGTGTGC9GENIChomozygous135463384
1227122612227122613TC14GENIChomozygous135822682
1227125803227125817ACATACATACACAT17GENIChomozygous142795401
1227126997227126998AG10GENIChomozygous147394413
1227127140227127141GA10GENICpossibly homozygous142867803
1227131053227131054TA18GENIChomozygous135822686
1227131280227131281TG13GENIChomozygous142867804
1227133869227133870CT24GENIChomozygous142867805
1227134131227134132AG18GENICpossibly homozygous142867806
1227134435227134436CA15GENIChomozygous135822689
1227134624227134625AG18GENIChomozygous135822690
1227135211227135211ATCCATCCATCC23GENICheterozygous145248448
1227135215227135215ATCCATCCATCCATCC15GENICpossibly homozygous142795402
1227135886227135887GA17GENIChomozygous135822691
1227135972227135973CT14GENIChomozygous142867807
1227126997227126998A10GENICheterozygous404053896
1227127140227127141G10GENICheterozygous404053897