chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 90733464 90733465 G GT 18 GENIC homozygous 733732507 9 90733496 90733497 G GT 22 GENIC homozygous 733732508 9 90735882 90735884 GT -- 11 GENIC heterozygous 733732509 9 90736030 90736031 T TGGGA 15 GENIC homozygous 733732513 9 90736032 90736033 T G 16 GENIC homozygous 607761829 9 90736878 90736879 T G 21 GENIC homozygous 606715495 9 90736921 90736922 T G 20 GENIC homozygous 606715496 9 90736932 90736933 T G 20 GENIC homozygous 606715497 9 90736946 90736947 A G 25 GENIC homozygous 606715498 9 90736954 90736955 T G 24 GENIC homozygous 606715499 9 90736971 90736972 T A 28 GENIC homozygous 606715500 9 90738562 90738563 T C 13 GENIC homozygous 607761830 9 90738801 90738802 C - 1 GENIC homozygous 733732514 9 90738817 90738818 T - 1 GENIC homozygous 733732515 9 90740610 90740612 AT -- 2 GENIC homozygous 733732516 9 90741455 90741456 A AAGG 12 GENIC homozygous 733732517 9 90742426 90742428 AA -- 5 GENIC heterozygous 733732518 9 90742583 90742584 C T 12 GENIC homozygous 607761831 9 90742585 90742586 T C 12 GENIC homozygous 607761832 9 90742599 90742600 C A 12 GENIC homozygous 607761833 9 90742601 90742602 G T 13 GENIC homozygous 607761834 9 90742604 90742606 CC -- 14 GENIC homozygous 733732519 9 90742610 90742611 C T 15 GENIC homozygous 607761835 9 90742611 90742612 C A 16 GENIC homozygous 607761836 9 90742808 90742809 A AG 5 GENIC homozygous 733732520 9 90747690 90747691 T TAG 11 GENIC homozygous 733732521 9 90747950 90747951 C T 10 GENIC homozygous 607761837 9 90748679 90748680 C CGTGT 3 GENIC heterozygous 733732524 9 90748694 90748696 GT -- 3 GENIC heterozygous 733732523 9 90749563 90749564 G GT 6 GENIC heterozygous 733732525