chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 103657968 103657969 A G 26 GENIC homozygous 642436687 10 103658439 103658440 A G 30 GENIC homozygous 642436688 10 103658665 103658666 C T 30 GENIC homozygous 642436689 10 103659475 103659476 A C 29 GENIC homozygous 642436690 10 103662334 103662335 C - 9 GENIC possibly homozygous 752572373 10 103662601 103662602 C CT 18 GENIC possibly homozygous 752572374 10 103665767 103665768 A G 33 GENIC homozygous 642436691 10 103667623 103667624 C T 31 GENIC homozygous 642436692 10 103667793 103667794 A G 34 GENIC homozygous 642436693 10 103667854 103667855 A G 17 GENIC homozygous 642436694 10 103668206 103668210 GTGT ---- 23 GENIC homozygous 752572375 10 103668541 103668543 AA -- 18 GENIC homozygous 752572376 10 103669968 103669969 C T 27 GENIC homozygous 642436695 10 103670372 103670373 C T 23 GENIC homozygous 642436696