chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 80699798 80699799 G A 32 GENIC possibly homozygous 995509922 18 80700019 80700020 C T 27 GENIC possibly homozygous 995509923 18 80700111 80700112 A G 29 GENIC possibly homozygous 995509924 18 80700122 80700123 G A 27 GENIC possibly homozygous 995509925 18 80700257 80700258 A G 26 GENIC possibly homozygous 995509926 18 80700361 80700362 A G 28 GENIC homozygous 995509927 18 80700464 80700465 G A 22 GENIC homozygous 995509928 18 80700526 80700527 A G 23 GENIC homozygous 995509929 18 80700682 80700683 G C 23 GENIC homozygous 995509930 18 80700819 80700820 T C 36 GENIC possibly homozygous 995509931 18 80700978 80700979 C T 23 GENIC possibly homozygous 995509932 18 80701179 80701180 G C 23 GENIC possibly homozygous 995509933 18 80701185 80701186 C G 24 GENIC possibly homozygous 995509934 18 80703803 80703804 C T 19 GENIC homozygous 995509935 18 80705728 80705729 G A 25 GENIC possibly homozygous 995509936 18 80705985 80705986 G A 24 GENIC possibly homozygous 995509937 18 80706751 80706752 A C 26 GENIC possibly homozygous 995509938 18 80714022 80714023 A G 20 GENIC homozygous 995509939 18 80718797 80718798 T C 16 GENIC homozygous 995509940 18 80720267 80720268 T G 32 GENIC homozygous 995509941 18 80720851 80720852 T C 35 GENIC possibly homozygous 995509942