chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 90733464 90733465 G GT 23 GENIC homozygous 750008610 9 90733496 90733497 G GT 34 GENIC homozygous 750008611 9 90733831 90733832 C CGT 11 GENIC homozygous 750008614 9 90735881 90735882 A AGT 18 GENIC possibly homozygous 750008616 9 90736030 90736031 T TGGGA 38 GENIC homozygous 750008619 9 90736032 90736033 T G 38 GENIC homozygous 638455957 9 90736878 90736879 T G 27 GENIC homozygous 638455958 9 90736921 90736922 T G 23 GENIC homozygous 638455959 9 90736932 90736933 T G 25 GENIC homozygous 638455960 9 90736946 90736947 A G 27 GENIC homozygous 638455961 9 90736954 90736955 T G 28 GENIC homozygous 638455962 9 90736971 90736972 T A 27 GENIC homozygous 638455963 9 90738562 90738563 T C 16 GENIC homozygous 638455964 9 90741455 90741456 A AAGG 7 GENIC homozygous 750008620 9 90742426 90742428 AA -- 21 GENIC heterozygous 750008621 9 90742583 90742584 C T 27 GENIC possibly homozygous 638455965 9 90742585 90742586 T C 29 GENIC possibly homozygous 638455966 9 90742599 90742600 C A 30 GENIC homozygous 638455967 9 90742601 90742602 G T 30 GENIC homozygous 638455968 9 90742604 90742606 CC -- 32 GENIC homozygous 750008622 9 90742610 90742611 C T 32 GENIC homozygous 638455969 9 90742611 90742612 C A 31 GENIC homozygous 638455970 9 90742808 90742809 A AG 1 GENIC homozygous 750008623 9 90747690 90747691 T - 2 GENIC homozygous 750008624 9 90747693 90747702 GTTGTTGTT --------- 2 GENIC homozygous 750008625 9 90747950 90747951 C T 32 GENIC homozygous 638455971 9 90748679 90748680 C CGTGT 15 GENIC homozygous 750008628