chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 90733464 90733465 G GT 18 GENIC homozygous 747809916 9 90733496 90733497 G GT 23 GENIC homozygous 747809917 9 90733831 90733832 C CGT 7 GENIC possibly homozygous 747809920 9 90735881 90735882 A AGT 18 GENIC heterozygous 747809922 9 90735881 90735882 A AGTGT 18 GENIC heterozygous 747809923 9 90735882 90735884 GT -- 18 GENIC heterozygous 747809921 9 90736030 90736031 T TGGGA 42 GENIC homozygous 747809925 9 90736032 90736033 T G 42 GENIC homozygous 635018020 9 90736878 90736879 T G 16 GENIC homozygous 635018021 9 90736921 90736922 T G 22 GENIC homozygous 635018022 9 90736932 90736933 T G 24 GENIC homozygous 635018023 9 90736946 90736947 A G 26 GENIC homozygous 635018024 9 90736954 90736955 T G 27 GENIC homozygous 635018025 9 90736971 90736972 T A 30 GENIC homozygous 635018026 9 90738562 90738563 T C 2 GENIC homozygous 635018027 9 90741455 90741456 A AAGG 11 GENIC homozygous 747809926 9 90742426 90742428 AA -- 14 GENIC heterozygous 747809927 9 90742583 90742584 C T 14 GENIC possibly homozygous 635018028 9 90742585 90742586 T C 14 GENIC possibly homozygous 635018029 9 90742599 90742600 C A 18 GENIC homozygous 635018030 9 90742601 90742602 G T 18 GENIC homozygous 635018031 9 90742604 90742606 CC -- 18 GENIC homozygous 747809928 9 90742610 90742611 C T 20 GENIC homozygous 635018032 9 90742611 90742612 C A 20 GENIC homozygous 635018033 9 90742808 90742809 A AG 6 GENIC homozygous 747809929 9 90747690 90747691 T - 7 GENIC homozygous 747809930 9 90747693 90747702 GTTGTTGTT --------- 8 GENIC homozygous 747809931 9 90747950 90747951 C T 38 GENIC homozygous 635018034 9 90748679 90748680 C CGTGT 4 GENIC homozygous 747809934