chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 90733464 90733465 G GT 21 GENIC homozygous 752160683 9 90733496 90733497 G GT 25 GENIC homozygous 752160684 9 90735882 90735884 GT -- 14 GENIC heterozygous 752160685 9 90736030 90736031 T TGGGA 10 GENIC homozygous 752160689 9 90736032 90736033 T G 10 GENIC homozygous 641835115 9 90736878 90736879 T G 22 GENIC homozygous 641835116 9 90736921 90736922 T G 22 GENIC homozygous 641835117 9 90736932 90736933 T G 22 GENIC homozygous 641835118 9 90736946 90736947 A G 18 GENIC homozygous 641835119 9 90736954 90736955 T G 18 GENIC homozygous 641835120 9 90736971 90736972 T A 15 GENIC homozygous 641835121 9 90738562 90738563 T C 21 GENIC homozygous 641835122 9 90741455 90741456 A AAGG 9 GENIC homozygous 752160690 9 90742426 90742428 AA -- 1 GENIC homozygous 752160691 9 90742583 90742584 C T 19 GENIC homozygous 641835123 9 90742585 90742586 T C 19 GENIC homozygous 641835124 9 90742599 90742600 C A 21 GENIC homozygous 641835125 9 90742601 90742602 G T 22 GENIC homozygous 641835126 9 90742604 90742606 CC -- 22 GENIC homozygous 752160692 9 90742610 90742611 C T 25 GENIC homozygous 641835127 9 90742611 90742612 C A 25 GENIC homozygous 641835128 9 90742808 90742809 A AG 2 GENIC homozygous 752160693 9 90747690 90747691 T TAG 10 GENIC homozygous 752160694 9 90747950 90747951 C T 11 GENIC homozygous 641835129 9 90748679 90748680 C CGTGT 6 GENIC heterozygous 752160697