chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 2550985 2550986 T C 22 GENIC homozygous 976001827 7 2552990 2552991 C T 20 GENIC homozygous 976001828 7 2554819 2554820 T C 15 GENIC homozygous 976001829 7 2554878 2554879 A G 30 GENIC homozygous 976001830 7 2563234 2563235 G C 8 GENIC homozygous 976001831 7 2567244 2567245 G A 15 GENIC homozygous 976001832 7 2568260 2568261 A T 27 GENIC homozygous 976001833 7 2569793 2569794 C T 17 GENIC homozygous 976001834 7 2571932 2571933 A G 21 GENIC homozygous 976001835 7 2572991 2572992 T A 25 GENIC homozygous 976001836 7 2573235 2573236 T C 27 GENIC homozygous 976001837 7 2577937 2577938 A T 19 GENIC homozygous 976001838 7 2577938 2577939 T A 19 GENIC homozygous 976001839 7 2581932 2581933 C T 11 GENIC homozygous 976001840 7 2586483 2586484 C T 17 GENIC homozygous 976001841 7 2586776 2586777 T C 33 GENIC homozygous 976001842 7 2591499 2591500 C T 9 GENIC homozygous 976001843