chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204945401204945402GA18GENIChomozygous61063703
1204947591204947592CT7GENIChomozygous62030196
1204948638204948639CCA7GENIChomozygous62030197
1204948686204948687GT9GENIChomozygous61063707
1204949240204949241CT11GENIChomozygous61063715
1204949814204949816CA--12GENIChomozygous61063716
1204950171204950172AG21GENIChomozygous61063717
1204950370204950371GA19GENIChomozygous61063718
1204950810204950811CT21GENIChomozygous61063719
1204950952204950953GT14GENIChomozygous62030198
1204951240204951241AG18GENIChomozygous61063720
1204951241204951242AG18GENIChomozygous61063721
1204951243204951244TG18GENIChomozygous61063722
1204951278204951279GA21GENIChomozygous62030199
1204951921204951924CTT---12GENIChomozygous61063725
1204953346204953347GT15GENIChomozygous61063726
1204954299204954300TC21GENIChomozygous61063727
1204955456204955457GA16GENIChomozygous61063728
1204955999204956000TC13GENIChomozygous61063732
1204956076204956077CT10GENIChomozygous61063733
1204956153204956154CT8GENIChomozygous61063735
1204957835204957836GA10GENIChomozygous61063737
1204958019204958020AT19GENIChomozygous61063738
1204960540204960541GA19GENICheterozygous61063742
1204960611204960612CT82GENICheterozygous61063743
1204960618204960619GT87GENICheterozygous61063744
1204960631204960632CT88GENICheterozygous61063745
1204960635204960636AG83GENICpossibly homozygous61063746
1204960651204960652CG94GENICpossibly homozygous61063747
1204960661204960662GGGA86GENICpossibly homozygous61063748
1204961380204961381AG62GENICpossibly homozygous61063755
1204961384204961385TC61GENICpossibly homozygous61063756