chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122415972024159721GC15GENICheterozygous50371465
122416022324160224TTA15GENICpossibly homozygous50131911
122416025024160251TC22GENIChomozygous50131913
122416109424161095TA27GENIChomozygous50131915
122416109724161098CT28GENIChomozygous50131917
122416138824161389GT23GENIChomozygous50131919
122416185924161860CT23GENICheterozygous50131921
122416198824161989TC14GENIChomozygous50131923
122416232424162325GT19GENIChomozygous50131925
122416240224162403TA30GENICpossibly homozygous50131927
122416359024163591AG31GENIChomozygous50131929
122416377124163772CT20GENIChomozygous50131931
122416444624164447TC20GENIChomozygous50131933
122416447124164472CT19GENIChomozygous50131935
122416459724164598GA21GENIChomozygous50131937
122416461824164619TC19GENIChomozygous50131939
122416511424165126ACACACACATAT------------19GENIChomozygous50131941
122416538524165386AG22GENIChomozygous50131943
122416557424165575TA21GENIChomozygous50131946
122416581524165816AG16GENIChomozygous50131948
122416606124166062CT19GENIChomozygous50131950
122416634924166350CT19GENIChomozygous50131952
122416668824166689GC21GENIChomozygous50131954
122416721524167216GA26GENIChomozygous50131956
122416800424168005GA19GENIChomozygous50131965
122416753524167536CT23GENIChomozygous50131958
122416770724167708AG27GENIChomozygous50131960
122416774824167749AG26GENIChomozygous50131962
122416816824168169T-7GENICheterozygous50131966
122416891524168916TTTGTC21GENIChomozygous50131968
122416895224168953TC23GENIChomozygous50131970
122416940324169404TC22GENIChomozygous50131972
122417030724170308GA15GENICpossibly homozygous50131974
122417035424170355CT15GENICpossibly homozygous50131977
122417036124170362AACC3GENIChomozygous50131979
122417051824170519GA19GENIChomozygous50131983