chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	33156693	33156694	C	T	49	GENIC	homozygous	112671875
15	33156728	33156729	G	C	46	GENIC	homozygous	112671877
15	33156735	33156736	A	C	46	GENIC	homozygous	112671879
15	33157340	33157341	G	A	60	GENIC	homozygous	112671881
15	33157471	33157472	C	T	38	GENIC	homozygous	112671883
15	33157787	33157788	G	A	47	GENIC	homozygous	112671885
15	33157915	33157916	G	A	70	GENIC	homozygous	112671887
15	33158959	33158960	G	T	59	GENIC	homozygous	112671889
15	33159146	33159147	T	C	57	GENIC	homozygous	112671891
15	33159755	33159756	G	T	69	GENIC	possibly homozygous	112671893
15	33159819	33159820	T	C	72	GENIC	homozygous	112671894
15	33158984	33158984		AGAC	42	GENIC	possibly homozygous	131159161
15	33159325	33159326	G		69	GENIC	homozygous	131159162
15	33159916	33159916		A	51	GENIC	homozygous	131159163
15	33160320	33160321	T	G	63	GENIC	homozygous	112671896
15	33160577	33160578	T	C	57	GENIC	homozygous	112671898
15	33161723	33161724	A	G	56	GENIC	homozygous	112671900
15	33161756	33161757	G	A	62	GENIC	homozygous	112671902
15	33161833	33161834	C	A	69	GENIC	homozygous	112671904
15	33164899	33164899		AGAA	38	GENIC	homozygous	131159164
15	33165247	33165248	C	T	48	GENIC	homozygous	112671906