chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 125042349 125042350 A T 34 GENIC homozygous 975970855 6 125043149 125043150 G T 20 GENIC homozygous 975970856 6 125045107 125045108 C T 28 GENIC homozygous 975970857 6 125048772 125048773 G A 48 GENIC homozygous 975970858 6 125049812 125049813 T C 31 GENIC homozygous 975970859 6 125051702 125051703 T C 36 GENIC homozygous 975970860 6 125051787 125051788 G A 41 GENIC homozygous 975970861 6 125052674 125052675 C T 19 GENIC homozygous 975970862 6 125052929 125052930 C T 24 GENIC homozygous 975970863 6 125053620 125053621 A G 33 GENIC homozygous 975970864 6 125054104 125054105 C T 43 GENIC homozygous 975970865 6 125058255 125058256 G A 16 GENIC homozygous 975970866 6 125061110 125061111 G T 17 GENIC homozygous 975970867 6 125064989 125064990 G A 14 GENIC possibly homozygous 975970868 6 125066295 125066296 T C 20 GENIC homozygous 975970869 6 125067010 125067011 A C 25 GENIC homozygous 975970870 6 125067989 125067990 C T 22 GENIC homozygous 975970871 6 125068238 125068239 C T 30 GENIC homozygous 975970872 6 125068645 125068646 C T 46 GENIC homozygous 975970873 6 125069020 125069021 T C 25 GENIC homozygous 975970874 6 125069192 125069193 C G 18 GENIC homozygous 975970875 6 125070462 125070463 G A 45 GENIC homozygous 975970876 6 125070954 125070955 C T 33 GENIC homozygous 975970877 6 125072010 125072011 G C 19 GENIC homozygous 975970878 6 125073846 125073847 C T 21 GENIC homozygous 975970879 6 125075490 125075491 G A 19 GENIC homozygous 975970880 6 125077163 125077164 T A 26 GENIC homozygous 975970881 6 125078090 125078091 A G 29 GENIC homozygous 975970882 6 125081226 125081227 A C 30 GENIC homozygous 975970883