chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 243160892 243160893 C T 72 GENIC homozygous 111384387 2 243163914 243163915 T 56 GENIC homozygous 132810542 2 243163932 243163933 A G 59 GENIC homozygous 110345908 2 243163989 243163990 T G 49 GENIC homozygous 120247385 2 243164025 243164026 C T 45 GENIC homozygous 111384391 2 243165800 243165801 T C 37 GENIC homozygous 110345912 2 243165974 243165975 C A 40 GENIC homozygous 110345914 2 243165029 243165033 TTTC 30 GENIC homozygous 127756889 2 243165899 243165900 C A 26 GENIC homozygous 132819936 2 243166444 243166445 T C 50 GENIC homozygous 110345916 2 243166502 243166503 C A 45 GENIC homozygous 120247386 2 243167540 243167541 T C 44 GENIC homozygous 110345922 2 243167642 243167642 TG 44 GENIC possibly homozygous 132810543 2 243167933 243167934 T C 56 GENIC homozygous 120247387 2 243168084 243168085 C G 67 GENIC homozygous 110913301 2 243168823 243168824 G A 49 GENIC homozygous 110345928 2 243168920 243168925 TAGTA 48 GENIC homozygous 127756891 2 243169511 243169512 C G 46 GENIC homozygous 110345930 2 243170265 243170266 A G 61 GENIC homozygous 110345932 2 243170706 243170707 A T 29 GENIC homozygous 110345934 2 243170719 243170720 G A 29 GENIC possibly homozygous 111032608 2 243170720 243170721 C T 29 GENIC possibly homozygous 111032610 2 243170722 243170723 G A 30 GENIC possibly homozygous 111032612 2 243170735 243170736 A G 30 GENIC possibly homozygous 121620845 2 243170759 243170760 T C 31 GENIC possibly homozygous 110845327 2 243170773 243170774 A G 27 GENIC possibly homozygous 110633125 2 243170801 243170802 T C 24 GENIC possibly homozygous 110345936 2 243170816 243170817 G C 29 GENIC possibly homozygous 110345938 2 243171116 243171117 A G 46 GENIC homozygous 132819937 2 243171900 243171901 A C 64 GENIC possibly homozygous 110345940 2 243172627 243172628 G 73 GENIC possibly homozygous 132810544