chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	203928665	203928666	A	C	20	GENIC	homozygous	141431654
2	203929577	203929578	C	T	20	GENIC	homozygous	141431655
2	203930556	203930557	T	G	6	GENIC	homozygous	141431656
2	203932269	203932270	T	C	18	GENIC	homozygous	136446038
2	203934050	203934051	A	G	22	GENIC	homozygous	136446041
2	203935914	203935915	C	T	21	GENIC	homozygous	141431657
2	203936239	203936240	G	C	19	GENIC	homozygous	141431658
2	203936603	203936604	A	G	24	GENIC	homozygous	141431659
2	203936758	203936759	C	A	23	GENIC	homozygous	141431660
2	203936859	203936860	T	C	23	GENIC	homozygous	141431661
2	203937062	203937063	T	A	14	GENIC	homozygous	141431662
2	203937684	203937685	C	T	14	GENIC	homozygous	141431663
2	203937944	203937945	G	A	34	GENIC	homozygous	141431664
2	203938102	203938103	A	C	21	GENIC	homozygous	141431665
2	203943820	203943821	T	C	18	GENIC	possibly homozygous	136446047
2	203943974	203943975	C	A	11	GENIC	homozygous	141431666
2	203944048	203944049	T	C	13	GENIC	homozygous	136446048
2	203945618	203945619	C	T	10	GENIC	homozygous	141431667
2	203946632	203946633	T	C	9	GENIC	homozygous	136446051
2	203946659	203946660	A	T	14	GENIC	homozygous	141431668
2	203933994	203933995	G	A	18	GENIC	homozygous	149210264
2	203936927	203936938	TGGGGCGGAGC		18	GENIC	homozygous	141336170
2	203946210	203946210		TTTG	9	GENIC	homozygous	149201010