chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25928760 25928761 A G 9 GENIC homozygous 950726871 13 25928763 25928764 A G 9 GENIC homozygous 950726872 13 25928766 25928767 A G 15 GENIC homozygous 950726873 13 25929592 25929593 G C 6 GENIC homozygous 950726874 13 25930014 25930015 C G 27 GENIC homozygous 950726875 13 25932098 25932099 A G 16 GENIC homozygous 950726876 13 25933968 25933969 A G 14 GENIC homozygous 950726877 13 25934709 25934710 G T 16 GENIC homozygous 950726878 13 25935708 25935709 C T 27 GENIC homozygous 950726879 13 25935922 25935923 G A 16 GENIC homozygous 950726880 13 25939690 25939691 C T 16 GENIC homozygous 950726881 13 25939981 25939982 C G 22 GENIC homozygous 950726882 13 25940180 25940181 C A 22 GENIC homozygous 950726883 13 25940369 25940370 G A 23 GENIC homozygous 950726884 13 25941095 25941096 T C 15 GENIC homozygous 950726885 13 25941195 25941196 C A 22 GENIC homozygous 950726886 13 25941208 25941209 C T 20 GENIC homozygous 950726887 13 25941736 25941737 A G 19 GENIC homozygous 950726888 13 25942084 25942085 C T 10 GENIC homozygous 950726889 13 25943081 25943082 G A 19 GENIC homozygous 950726890 13 25945548 25945549 C T 16 GENIC homozygous 950726891 13 25949824 25949825 T A 16 GENIC homozygous 950726892