chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 7380657 7380658 T TAC 10 GENIC heterozygous 716818894 X 7380941 7380942 T TA 41 GENIC homozygous 716818895 X 7381718 7381719 C T 20 GENIC homozygous 578014744 X 7389369 7389370 T TC 18 GENIC homozygous 716818896 X 7391568 7391569 A AT 7 GENIC homozygous 716818897 X 7403400 7403401 T - 19 GENIC heterozygous 716818898 X 7404069 7404070 T C 18 GENIC homozygous 578014745 X 7413056 7413057 C CATAGATAG 5 GENIC homozygous 716818901 X 7418485 7418486 A ATTTCTTTC 11 GENIC heterozygous 716818903 X 7418485 7418486 A ATTTCTTTCTTTC 11 GENIC heterozygous 716818904 X 7418634 7418635 C CGTGT 19 GENIC possibly homozygous 716818905 X 7420680 7420681 G T 29 GENIC homozygous 578014746 X 7420686 7420687 G T 29 GENIC homozygous 578014747 X 7420690 7420691 T - 29 GENIC homozygous 716818906 X 7431235 7431236 A T 29 GENIC homozygous 578014748 X 7432921 7432927 TGTGTG ------ 2 GENIC homozygous 716818907 X 7433665 7433666 T - 26 GENIC homozygous 716818909 X 7436725 7436726 A - 13 GENIC homozygous 716818910 X 7437042 7437043 A C 22 GENIC homozygous 578014749