chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122416025024160251TC28GENIChomozygous50131913
122416103024161031CA43GENIChomozygous50439047
122416109424161095TA35GENIChomozygous50131915
122416109724161098CT34GENIChomozygous50131917
122416181524161816TTCG15GENIChomozygous50439049
122416181624161817AATC17GENICheterozygous50538425
122416181624161817AATCTC17GENICheterozygous50538426
122416198824161989TC38GENIChomozygous50131923
122416240224162403TA28GENIChomozygous50131927
122416270824162709TA38GENIChomozygous50439051
122416359024163591AG44GENIChomozygous50131929
122416377124163772CT43GENICpossibly homozygous50131931
122416444624164447TC56GENIChomozygous50131933
122416447124164472CT49GENIChomozygous50131935
122416459724164598GA46GENIChomozygous50131937
122416461824164619TC42GENIChomozygous50131939
122416508524165086AAAC14GENICheterozygous50538427
122416512324165124TC17GENIChomozygous50538428
122416512524165126TC17GENIChomozygous50538429
122416538524165386AG33GENIChomozygous50131943
122416557424165575TA33GENIChomozygous50131946
122416581524165816AG31GENIChomozygous50131948
122416634924166350CT39GENIChomozygous50131952
122416668824166689GC21GENIChomozygous50131954
122416721524167216GA44GENIChomozygous50131956
122416741824167419CT53GENIChomozygous50439053
122416753524167536CT41GENIChomozygous50131958
122416770724167708AG39GENIChomozygous50131960
122416774824167749AG46GENIChomozygous50131962
122416800424168005GA24GENIChomozygous50131965
122416891524168916TTTGTC22GENIChomozygous50131968
122416895224168953TC19GENIChomozygous50131970
122416940324169404TC44GENIChomozygous50131972
122417030724170308GA15GENIChomozygous50131974
122417035424170355CT11GENIChomozygous50131977
122417036124170362AACC5GENICheterozygous50131979
122417051824170519GA18GENIChomozygous50131983
122416508524165086AAACAC14GENICpossibly homozygous50292652