chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1269285416269285417AT18GENIChomozygous61210790
1269286770269286771CT42GENIChomozygous61210792
1269287497269287498CCGT17GENICheterozygous61210794
1269287497269287498CCGTGT17GENICheterozygous61210796
1269287497269287498CCGTGTGT17GENICheterozygous62215228
1269287892269287893GA27GENIChomozygous61210798
1269288942269288943AG38GENIChomozygous61210800
1269292168269292169GA45GENIChomozygous61210802
1269293012269293013CT35GENIChomozygous61210804
1269294274269294275TC46GENIChomozygous61210806
1269294393269294394CT53GENIChomozygous61210808
1269294932269294948CTACTGCCCCAGTGCT----------------37GENIChomozygous61210810
1269295131269295136GCACA-----39GENIChomozygous61210812
1269295763269295764GA34GENIChomozygous61210814
1269295929269295930GT39GENIChomozygous61210816
1269296058269296059GA39GENIChomozygous61210818
1269298741269298761ACACACACACACACACACAC--------------------26GENIChomozygous61210828
1269298904269298905CCAT41GENIChomozygous61210832
1269299859269299860GA34GENIChomozygous61210834
1269300565269300566AT39GENIChomozygous61210836
1269300568269300569AT36GENIChomozygous61210838
1269301187269301188CT39GENIChomozygous61210840