chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 85684955 85684956 T G 29 GENIC homozygous 953088595 10 85685439 85685440 A G 27 GENIC homozygous 953088596 10 85685811 85685812 T C 28 GENIC homozygous 953088597 10 85686161 85686162 A G 30 GENIC homozygous 953088598 10 85686829 85686830 C T 26 GENIC homozygous 953088599 10 85687564 85687565 C G 11 GENIC homozygous 953088600 10 85689557 85689558 A G 25 GENIC homozygous 953088601 10 85689974 85689975 G A 17 GENIC homozygous 953088602 10 85689987 85689988 G A 20 GENIC homozygous 953088603 10 85690306 85690307 G A 24 GENIC homozygous 953088604 10 85692742 85692743 C T 26 GENIC homozygous 953088605 10 85693669 85693670 G A 20 GENIC homozygous 953088606 10 85693963 85693964 T C 16 GENIC homozygous 953088607 10 85697768 85697769 T C 28 GENIC homozygous 953088608 10 85699346 85699347 C T 17 GENIC homozygous 953088609 10 85702549 85702550 T C 27 GENIC homozygous 953088610 10 85702839 85702840 A G 18 GENIC homozygous 953088611 10 85706674 85706675 C A 28 GENIC homozygous 953088612 10 85707478 85707479 G A 22 GENIC homozygous 953088613