chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	226581748	226581749	C	T	35	GENIC	possibly homozygous	74422188
2	226581770	226581771	C	A	33	GENIC	possibly homozygous	74422191
2	226581787	226581788	C	G	29	GENIC	possibly homozygous	74422194
2	226581831	226581832	A	G	23	GENIC	possibly homozygous	74422197
2	226581980	226581981	G	A	16	GENIC	possibly homozygous	75716548
2	226582886	226582887	A	G	28	GENIC	possibly homozygous	74422200
2	226583585	226583586	G	C	23	GENIC	homozygous	74422203
2	226586308	226586309	C	T	31	GENIC	homozygous	74422212
2	226587018	226587019	G	A	16	GENIC	possibly homozygous	74422218
2	226587203	226587204	C	A	19	GENIC	possibly homozygous	75716550
2	226588189	226588190	C	T	24	GENIC	homozygous	75716556
2	226588526	226588527	C	T	32	GENIC	homozygous	74422227
2	226589566	226589567	A	C	19	GENIC	homozygous	75716558
2	226590916	226590917	T	G	19	GENIC	possibly homozygous	74422233
2	226593899	226593900	G	T	31	GENIC	homozygous	74422251
2	226595783	226595784	C	T	5	GENIC	homozygous	75716567
2	226596535	226596536	T	A	26	GENIC	possibly homozygous	75716569
2	226597654	226597655	A	G	17	GENIC	homozygous	74422266
2	226597738	226597739	G	A	11	GENIC	possibly homozygous	74422269
2	226597792	226597793	G	A	15	GENIC	homozygous	75716571
2	226598656	226598657	G	T	17	GENIC	homozygous	74933586
2	226598781	226598782	A	T	25	GENIC	homozygous	74933587
2	226599804	226599805	C	G	24	GENIC	possibly homozygous	75716573
2	226599879	226599880	G	A	16	GENIC	homozygous	74933590
2	226599889	226599890	T	C	17	GENIC	homozygous	74933591