chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 59490878 59490879 T A 17 GENIC homozygous 996996073 5 59492425 59492426 A G 15 GENIC homozygous 996996074 5 59496242 59496243 A G 31 GENIC homozygous 996996075 5 59496492 59496493 C A 14 GENIC homozygous 996996076 5 59496507 59496508 G A 12 GENIC homozygous 996996077 5 59498256 59498257 G A 32 GENIC homozygous 996996078 5 59499643 59499644 T A 29 GENIC homozygous 996996079 5 59500179 59500180 A G 21 GENIC homozygous 996996080 5 59501607 59501608 C T 23 GENIC homozygous 996996081 5 59502207 59502208 C A 27 GENIC homozygous 996996082 5 59502243 59502244 C T 23 GENIC homozygous 996996083 5 59502300 59502301 G A 29 GENIC homozygous 996996084 5 59502683 59502684 T C 21 GENIC homozygous 996996085 5 59502698 59502699 A T 21 GENIC homozygous 996996086 5 59503232 59503233 C T 20 GENIC homozygous 996996087 5 59503245 59503246 C T 21 GENIC homozygous 996996088 5 59503422 59503423 G A 21 GENIC homozygous 996996089 5 59503514 59503515 T C 19 GENIC homozygous 996996090 5 59504116 59504117 T C 12 GENIC homozygous 996996091 5 59504488 59504489 A G 18 GENIC homozygous 996996092 5 59504831 59504832 C A 24 GENIC homozygous 996996093 5 59504888 59504889 T C 28 GENIC homozygous 996996094 5 59505019 59505020 G T 26 GENIC homozygous 996996095 5 59505062 59505063 T A 22 GENIC homozygous 996996096 5 59505193 59505194 T C 23 GENIC homozygous 996996097 5 59505463 59505464 T C 13 GENIC homozygous 996996098 5 59505702 59505703 C T 22 GENIC homozygous 996996099 5 59505718 59505719 G A 16 GENIC homozygous 996996100 5 59505848 59505849 C T 18 GENIC homozygous 996996101 5 59505925 59505926 T C 17 GENIC homozygous 996996102 5 59506002 59506003 C T 23 GENIC homozygous 996996103 5 59506256 59506257 C T 16 GENIC homozygous 996996104 5 59506991 59506992 G C 16 GENIC homozygous 996996105