chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 95321491 95321492 A G 24 GENIC homozygous 109928110 2 95322499 95322500 A 18 GENIC homozygous 127654101 2 95322521 95322522 G 18 GENIC homozygous 127654102 2 95322543 95322543 C 19 GENIC homozygous 127654103 2 95322556 95322557 A 19 GENIC homozygous 127654104 2 95322561 95322562 G C 20 GENIC homozygous 109928112 2 95322570 95322571 G 21 GENIC homozygous 127654105 2 95322581 95322581 G 22 GENIC homozygous 127654106 2 95322585 95322585 C 21 GENIC homozygous 127654107 2 95322591 95322591 A 21 GENIC homozygous 127654108 2 95322598 95322599 A C 22 GENIC homozygous 121433062 2 95322615 95322616 G T 23 GENIC homozygous 109928114 2 95322619 95322619 A 23 GENIC homozygous 127654109 2 95322627 95322627 G 24 GENIC homozygous 127654110 2 95322652 95322653 G 21 GENIC homozygous 127654111 2 95322668 95322669 T 22 GENIC homozygous 127654112 2 95322679 95322680 T G 21 GENIC homozygous 109928116 2 95322685 95322685 C 22 GENIC homozygous 127654113 2 95322690 95322690 T 18 GENIC homozygous 127654114 2 95322695 95322695 C 16 GENIC homozygous 127654115 2 95322673 95322674 A G 23 GENIC homozygous 120251856 2 95322523 95322524 A G 18 GENIC homozygous 110571345 2 95322535 95322536 T G 18 GENIC homozygous 110571346 2 95322537 95322538 G T 17 GENIC homozygous 110571348 2 95322600 95322601 C T 22 GENIC homozygous 120350078 2 95322672 95322673 G A 23 GENIC homozygous 120251855