chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	49795998	49795999	G	T	18	GENIC	homozygous	58813746
2	49796719	49796720	A	T	13	GENIC	homozygous	58813747
2	49798437	49798438	A	T	13	GENIC	homozygous	58813748
2	49798488	49798489	A	G	11	GENIC	homozygous	58813749
2	49798797	49798798	C	T	17	GENIC	homozygous	58813751
2	49800154	49800160	ATATAT	------	13	GENIC	homozygous	59686030
2	49800595	49800596	A	G	11	GENIC	homozygous	58813753
2	49802324	49802325	A	T	12	GENIC	homozygous	58813755
2	49802397	49802398	T	C	13	GENIC	homozygous	58813756
2	49802398	49802399	A	G	13	GENIC	homozygous	58813757
2	49803862	49803866	CTGG	----	8	GENIC	homozygous	58813758
2	49804975	49804976	T	G	19	GENIC	possibly homozygous	58813759
2	49806347	49806348	C	T	17	GENIC	homozygous	58813761
2	49806482	49806483	G	A	15	GENIC	homozygous	59686036
2	49809495	49809496	C	G	9	GENIC	homozygous	58813770
2	49809996	49809997	G	A	11	GENIC	homozygous	58813772
2	49812430	49812431	T	A	9	GENIC	homozygous	59686046
2	49815277	49815278	A	-	17	GENIC	homozygous	58813776
2	49817515	49817516	T	G	15	GENIC	homozygous	58813778
2	49818038	49818039	A	G	14	GENIC	homozygous	58813779
2	49819614	49819615	A	G	11	GENIC	homozygous	58813780
2	49820359	49820360	C	T	7	GENIC	homozygous	58813782
2	49820364	49820365	A	C	8	GENIC	homozygous	58813783
2	49821620	49821621	A	-	8	GENIC	homozygous	59686060
2	49823343	49823344	A	G	15	GENIC	homozygous	59686064
2	49823808	49823809	C	G	11	GENIC	homozygous	59686066