chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6175387 6175388 A G 13 GENIC homozygous 933213085 14 6175517 6175518 T C 8 GENIC homozygous 933213086 14 6176768 6176769 A T 6 GENIC homozygous 933213087 14 6177149 6177150 T C 7 GENIC homozygous 933213088 14 6177400 6177401 G C 7 GENIC homozygous 933213089 14 6177456 6177457 T C 10 GENIC homozygous 933213090 14 6177559 6177560 A G 13 GENIC homozygous 933213091 14 6177626 6177627 A G 13 GENIC homozygous 933213092 14 6177826 6177827 A G 12 GENIC homozygous 933213093 14 6181139 6181140 G A 10 GENIC homozygous 933213094 14 6216600 6216601 C T 5 GENIC homozygous 933213095 14 6218929 6218930 C T 9 GENIC homozygous 933213096 14 6218963 6218964 C G 9 GENIC homozygous 933213097 14 6219311 6219312 C T 16 GENIC homozygous 933213098 14 6219445 6219446 G A 8 GENIC homozygous 933213099 14 6219600 6219601 G A 12 GENIC homozygous 933213100 14 6220214 6220215 C G 7 GENIC homozygous 933213101 14 6220406 6220407 G A 9 GENIC homozygous 933213102 14 6220714 6220715 A G 6 GENIC homozygous 933213103 14 6220981 6220982 A G 6 GENIC homozygous 933213104 14 6221230 6221231 T C 12 GENIC homozygous 933213105