chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 31242260 31242261 T C 58 GENIC homozygous 139266472 13 31243689 31243690 C T 37 GENIC homozygous 139266473 13 31244717 31244718 G 26 GENIC homozygous 139166888 13 31244808 31244809 T C 20 GENIC homozygous 139266474 13 31244970 31244971 T 29 GENIC possibly homozygous 139166889 13 31245285 31245328 AGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAA 18 GENIC homozygous 139166890 13 31245843 31245844 G C 63 GENIC homozygous 139266475 13 31245944 31245945 A G 63 GENIC homozygous 139266476 13 31246122 31246123 C G 42 GENIC homozygous 139266477 13 31246459 31246460 C T 47 GENIC homozygous 139266478 13 31247144 31247145 A G 41 GENIC homozygous 139266479 13 31247818 31247818 T 33 GENIC possibly homozygous 139166891 13 31247819 31247819 T 33 GENIC possibly homozygous 139166892 13 31248576 31248576 TT 63 GENIC homozygous 139166893 13 31248631 31248632 G T 65 GENIC homozygous 139266480 13 31248750 31248751 G A 47 GENIC homozygous 139266481 13 31249280 31249281 G T 53 GENIC homozygous 139266482 13 31249494 31249494 C 47 GENIC homozygous 139166894 13 31245250 31245251 C G 8 GENIC heterozygous 403334386 13 31245250 31245251 C 8 GENIC heterozygous 403334384 13 31245250 31245251 C T 8 GENIC heterozygous 403334385