chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 103657968 103657969 A G 35 GENIC homozygous 653843592 10 103658439 103658440 A G 21 GENIC homozygous 653843593 10 103658665 103658666 C T 26 GENIC homozygous 653843594 10 103659475 103659476 A C 36 GENIC homozygous 653843595 10 103662334 103662335 C - 7 GENIC homozygous 759370957 10 103662601 103662602 C CT 15 GENIC heterozygous 759370958 10 103662718 103662719 T - 14 GENIC heterozygous 759370960 10 103665767 103665768 A G 35 GENIC homozygous 653843596 10 103667623 103667624 C T 37 GENIC homozygous 653843597 10 103667793 103667794 A G 38 GENIC homozygous 653843598 10 103667854 103667855 A G 33 GENIC homozygous 653843599 10 103668206 103668210 GTGT ---- 27 GENIC homozygous 759370961 10 103668541 103668543 AA -- 23 GENIC homozygous 759370962 10 103669968 103669969 C T 28 GENIC homozygous 653843600 10 103670372 103670373 C T 30 GENIC homozygous 653843601