chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15986232	15986233	G	A	50	GENIC	homozygous	51770116
9	15987935	15987939	GGTC	----	14	GENIC	heterozygous	51770118
9	15987936	15987937	G	GT	21	GENIC	possibly homozygous	51770120
9	15988237	15988238	T	C	42	GENIC	possibly homozygous	51770122
9	15989920	15989921	A	-	2	GENIC	homozygous	51770124
9	15990185	15990186	C	CTT	22	GENIC	homozygous	51770126
9	15990210	15990211	C	T	31	GENIC	heterozygous	51770128
9	15994524	15994525	G	T	16	GENIC	possibly homozygous	51770130
9	15994529	15994530	G	T	15	GENIC	possibly homozygous	51770132
9	15994534	15994535	G	T	14	GENIC	possibly homozygous	51770134
9	15994549	15994550	G	T	14	GENIC	heterozygous	51770136
9	15994554	15994555	G	T	9	GENIC	possibly homozygous	51770139
9	15994559	15994560	G	T	11	GENIC	heterozygous	51770141
9	15994564	15994565	G	T	12	GENIC	heterozygous	51770143
9	15994579	15994580	T	G	15	GENIC	heterozygous	51770145
9	15994584	15994585	T	G	16	GENIC	heterozygous	51770147
9	15994911	15994912	T	C	41	GENIC	homozygous	51770149
9	15995199	15995200	A	G	55	GENIC	homozygous	51770151
9	15995247	15995248	T	C	66	GENIC	homozygous	51770153
9	15995248	15995249	G	A	63	GENIC	homozygous	51770155
9	15996023	15996024	A	G	48	GENIC	homozygous	51770157
9	15996196	15996197	G	A	46	GENIC	possibly homozygous	51770160
9	15997627	15997628	T	TCTC	43	GENIC	homozygous	51770162
9	15997808	15997809	C	-	35	GENIC	homozygous	51770164
9	15997851	15997852	T	TC	43	GENIC	homozygous	51770166
9	15998357	15998358	T	TGGACGCG	43	GENIC	homozygous	51770168
9	15999306	15999307	T	C	29	GENIC	homozygous	51770170
9	16000199	16000200	G	A	62	GENIC	possibly homozygous	51770172
9	16000847	16000848	G	A	51	GENIC	homozygous	51770174
9	16001035	16001036	T	C	64	GENIC	homozygous	51770176
9	16001364	16001365	T	C	70	GENIC	homozygous	51770178
9	16001584	16001585	G	A	46	GENIC	homozygous	51770180
9	16003471	16003472	A	G	62	GENIC	homozygous	51770182
9	16003900	16003901	A	G	31	GENIC	homozygous	51770184
9	16004332	16004333	C	T	34	GENIC	homozygous	51770186
9	16006748	16006749	A	G	41	GENIC	homozygous	51770188