chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6174916 6174917 G T 21 GENIC homozygous 991837890 14 6175387 6175388 A G 17 GENIC homozygous 991837891 14 6175388 6175389 G A 17 GENIC homozygous 991837892 14 6176768 6176769 A T 18 GENIC homozygous 991837893 14 6177149 6177150 T C 19 GENIC homozygous 991837894 14 6177400 6177401 G C 26 GENIC homozygous 991837895 14 6177456 6177457 T C 26 GENIC homozygous 991837896 14 6177559 6177560 A G 24 GENIC homozygous 991837897 14 6177626 6177627 A G 21 GENIC homozygous 991837898 14 6177826 6177827 A G 16 GENIC homozygous 991837899 14 6181139 6181140 G A 15 GENIC homozygous 991837900 14 6218929 6218930 C T 24 GENIC homozygous 991837901 14 6218963 6218964 C G 23 GENIC homozygous 991837902 14 6219311 6219312 C T 21 GENIC homozygous 991837903 14 6219445 6219446 G A 19 GENIC homozygous 991837904 14 6219600 6219601 G A 15 GENIC homozygous 991837905 14 6220214 6220215 C G 31 GENIC homozygous 991837906 14 6220223 6220224 C T 31 GENIC homozygous 991837907 14 6220406 6220407 G A 21 GENIC homozygous 991837908 14 6220981 6220982 A G 16 GENIC homozygous 991837909 14 6221230 6221231 T C 21 GENIC homozygous 991837910