chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 2550985 2550986 T C 28 GENIC homozygous 994018732 7 2552990 2552991 C T 24 GENIC homozygous 994018733 7 2554819 2554820 T C 32 GENIC possibly homozygous 994018734 7 2554878 2554879 A G 36 GENIC possibly homozygous 994018735 7 2563234 2563235 G C 25 GENIC homozygous 994018736 7 2567244 2567245 G A 18 GENIC possibly homozygous 994018737 7 2568260 2568261 A T 28 GENIC homozygous 994018738 7 2569793 2569794 C T 26 GENIC possibly homozygous 994018739 7 2571932 2571933 A G 20 GENIC possibly homozygous 994018740 7 2572991 2572992 T A 31 GENIC possibly homozygous 994018741 7 2573235 2573236 T C 20 GENIC possibly homozygous 994018742 7 2573891 2573892 G A 42 GENIC possibly homozygous 994018743 7 2581932 2581933 C T 25 GENIC homozygous 994018744 7 2586483 2586484 C T 23 GENIC homozygous 994018745 7 2586776 2586777 T C 32 GENIC possibly homozygous 994018746 7 2591499 2591500 C T 31 GENIC possibly homozygous 994018747