chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 90733464 90733465 G GT 25 GENIC homozygous 707533966 9 90733496 90733497 G GT 31 GENIC homozygous 707533967 9 90736030 90736031 T TGGGA 33 GENIC homozygous 707533968 9 90736032 90736033 T G 33 GENIC homozygous 560931024 9 90736878 90736879 T G 30 GENIC homozygous 559914670 9 90736921 90736922 T G 25 GENIC homozygous 559914671 9 90736932 90736933 T G 24 GENIC homozygous 559914672 9 90736946 90736947 A G 28 GENIC homozygous 559914673 9 90736954 90736955 T G 31 GENIC homozygous 559914674 9 90736971 90736972 T A 29 GENIC homozygous 559914675 9 90738562 90738563 T C 17 GENIC homozygous 560931025 9 90740610 90740612 AT -- 3 GENIC homozygous 707533969 9 90741455 90741456 A AAGG 13 GENIC homozygous 707533970 9 90742426 90742428 AA -- 7 GENIC homozygous 707533971 9 90742583 90742584 C T 17 GENIC homozygous 560931026 9 90742585 90742586 T C 18 GENIC homozygous 560931027 9 90742599 90742600 C A 26 GENIC homozygous 560931028 9 90742601 90742602 G T 27 GENIC homozygous 560931029 9 90742604 90742606 CC -- 27 GENIC homozygous 707533972 9 90742610 90742611 C T 28 GENIC homozygous 560931030 9 90742611 90742612 C A 28 GENIC homozygous 560931031 9 90742808 90742809 A AG 7 GENIC homozygous 707533973 9 90747690 90747691 T TAG 27 GENIC homozygous 707533974 9 90747950 90747951 C T 45 GENIC homozygous 560931032 9 90748679 90748680 C CGTGT 2 GENIC heterozygous 707533977 9 90749563 90749564 G GT 4 GENIC heterozygous 707533978