chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6175198 6175199 T G 14 GENIC homozygous 959094994 14 6175387 6175388 A G 13 GENIC homozygous 959094995 14 6175388 6175389 G A 14 GENIC homozygous 959094996 14 6176768 6176769 A T 15 GENIC homozygous 959094997 14 6177149 6177150 T C 21 GENIC homozygous 959094998 14 6177400 6177401 G C 33 GENIC homozygous 959094999 14 6177456 6177457 T C 33 GENIC homozygous 959095000 14 6177626 6177627 A G 28 GENIC homozygous 959095001 14 6177826 6177827 A G 27 GENIC homozygous 959095002 14 6181139 6181140 G A 13 GENIC homozygous 959095003 14 6216600 6216601 C T 16 GENIC homozygous 959095004 14 6218929 6218930 C T 28 GENIC homozygous 959095005 14 6218963 6218964 C G 35 GENIC homozygous 959095006 14 6219311 6219312 C T 16 GENIC homozygous 959095007 14 6219445 6219446 G A 27 GENIC possibly homozygous 959095008 14 6219600 6219601 G A 38 GENIC homozygous 959095009 14 6220214 6220215 C G 16 GENIC homozygous 959095010 14 6220223 6220224 C T 15 GENIC homozygous 959095011 14 6220406 6220407 G A 15 GENIC homozygous 959095012 14 6220550 6220551 T A 11 GENIC homozygous 959095013 14 6220564 6220565 G T 12 GENIC homozygous 959095014 14 6220714 6220715 A G 15 GENIC homozygous 959095015 14 6220747 6220748 T C 10 GENIC homozygous 959095016 14 6220981 6220982 A G 16 GENIC homozygous 959095017 14 6221230 6221231 T C 5 GENIC homozygous 959095018