chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6175517 6175518 T C 26 GENIC homozygous 986178823 14 6176768 6176769 A T 11 GENIC homozygous 986178824 14 6177149 6177150 T C 24 GENIC homozygous 986178825 14 6177400 6177401 G C 30 GENIC homozygous 986178826 14 6177456 6177457 T C 38 GENIC homozygous 986178827 14 6177559 6177560 A G 26 GENIC homozygous 986178828 14 6177626 6177627 A G 24 GENIC homozygous 986178829 14 6177826 6177827 A G 30 GENIC homozygous 986178830 14 6218280 6218281 C T 20 GENIC homozygous 986178831 14 6218929 6218930 C T 15 GENIC homozygous 986178832 14 6218963 6218964 C G 8 GENIC homozygous 986178833 14 6219311 6219312 C T 22 GENIC homozygous 986178834 14 6219445 6219446 G A 34 GENIC homozygous 986178835 14 6219600 6219601 G A 21 GENIC homozygous 986178836 14 6220214 6220215 C G 23 GENIC homozygous 986178837 14 6220223 6220224 C T 20 GENIC homozygous 986178838 14 6220406 6220407 G A 24 GENIC homozygous 986178839 14 6220981 6220982 A G 27 GENIC homozygous 986178840 14 6221230 6221231 T C 22 GENIC homozygous 986178841