chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 203928665 203928666 A C 44 GENIC homozygous 141431654 2 203929577 203929578 C T 55 GENIC homozygous 141431655 2 203930556 203930557 T G 17 GENIC possibly homozygous 141431656 2 203932269 203932270 T C 49 GENIC homozygous 136446038 2 203934050 203934051 A G 43 GENIC homozygous 136446041 2 203935914 203935915 C T 48 GENIC homozygous 141431657 2 203936239 203936240 G C 59 GENIC homozygous 141431658 2 203936603 203936604 A G 54 GENIC possibly homozygous 141431659 2 203936758 203936759 C A 65 GENIC possibly homozygous 141431660 2 203936859 203936860 T C 62 GENIC possibly homozygous 141431661 2 203936927 203936938 TGGGGCGGAGC 44 GENIC homozygous 141336170 2 203937062 203937063 T A 56 GENIC homozygous 141431662 2 203937684 203937685 C T 38 GENIC homozygous 141431663 2 203937944 203937945 G A 42 GENIC homozygous 141431664 2 203938102 203938103 A C 43 GENIC homozygous 141431665 2 203943820 203943821 T C 38 GENIC homozygous 136446047 2 203943974 203943975 C A 49 GENIC homozygous 141431666 2 203944048 203944049 T C 46 GENIC homozygous 136446048 2 203945618 203945619 C T 48 GENIC homozygous 141431667 2 203946632 203946633 T C 38 GENIC homozygous 136446051 2 203946659 203946660 A T 43 GENIC homozygous 141431668