chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 29289840 29289841 C G 11 GENIC homozygous 116540033 10 29290452 29290453 T C 76 GENIC possibly homozygous 116540035 10 29296144 29296145 C G 26 GENIC homozygous 117986110 10 29296402 29296403 C A 36 GENIC possibly homozygous 117986111 10 29296468 29296469 G C 38 GENIC homozygous 117986112 10 29296504 29296505 A G 28 GENIC homozygous 117327839 10 29296633 29296634 G C 37 GENIC homozygous 117001353 10 29296636 29296637 A G 41 GENIC homozygous 116540037 10 29296719 29296720 T G 44 GENIC homozygous 116540039 10 29300456 29300457 T C 74 GENIC homozygous 116540041 10 29304225 29304226 G T 42 GENIC homozygous 116540043 10 29314961 29314962 T G 18 GENIC heterozygous 116540047 10 29316320 29316321 A G 52 GENIC homozygous 116540049 10 29316541 29316542 T G 53 GENIC homozygous 116540051 10 29328612 29328613 T A 37 GENIC homozygous 116540053 10 29332764 29332765 T A 38 GENIC homozygous 116540057 10 29334886 29334887 G C 40 GENIC homozygous 116540059 10 29296784 29296785 G T 26 GENIC homozygous 116751139 10 29328978 29328979 C A 35 GENIC homozygous 116751141 10 29313543 29313544 G T 30 GENIC possibly homozygous 118080348