chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 90733464 90733465 G GT 17 GENIC homozygous 737831820 9 90733496 90733497 G GT 23 GENIC homozygous 737831821 9 90735881 90735882 A AGT 8 GENIC heterozygous 737831823 9 90735882 90735884 GT -- 8 GENIC heterozygous 737831822 9 90736030 90736031 T TGGGA 42 GENIC homozygous 737831826 9 90736032 90736033 T G 42 GENIC homozygous 614936151 9 90736878 90736879 T G 19 GENIC homozygous 613753892 9 90736921 90736922 T G 26 GENIC homozygous 613753893 9 90736932 90736933 T G 24 GENIC homozygous 613753894 9 90736946 90736947 A G 26 GENIC homozygous 613753895 9 90736954 90736955 T G 25 GENIC homozygous 613753896 9 90736971 90736972 T A 29 GENIC homozygous 613753897 9 90741455 90741456 A AAGG 8 GENIC homozygous 737831827 9 90742583 90742584 C T 2 GENIC homozygous 614936152 9 90742585 90742586 T C 5 GENIC homozygous 614936153 9 90742599 90742600 C A 9 GENIC homozygous 614936154 9 90742601 90742602 G T 10 GENIC homozygous 614936155 9 90742604 90742606 CC -- 11 GENIC homozygous 737831828 9 90742610 90742611 C T 15 GENIC homozygous 614936156 9 90742611 90742612 C A 19 GENIC homozygous 614936157 9 90747690 90747691 T TAG 1 GENIC homozygous 737831830 9 90747950 90747951 C T 11 GENIC homozygous 614936158