chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	33156693	33156694	C	T	34	GENIC	homozygous	112671875
15	33156728	33156729	G	C	30	GENIC	homozygous	112671877
15	33156735	33156736	A	C	31	GENIC	homozygous	112671879
15	33157340	33157341	G	A	35	GENIC	homozygous	112671881
15	33157471	33157472	C	T	29	GENIC	homozygous	112671883
15	33157787	33157788	G	A	39	GENIC	homozygous	112671885
15	33157915	33157916	G	A	35	GENIC	homozygous	112671887
15	33158959	33158960	G	T	47	GENIC	homozygous	112671889
15	33159146	33159147	T	C	43	GENIC	homozygous	112671891
15	33159755	33159756	G	T	37	GENIC	possibly homozygous	112671893
15	33159819	33159820	T	C	42	GENIC	possibly homozygous	112671894
15	33158984	33158984		AGAC	37	GENIC	homozygous	131159161
15	33159325	33159326	G		52	GENIC	homozygous	131159162
15	33159916	33159916		A	48	GENIC	homozygous	131159163
15	33160320	33160321	T	G	55	GENIC	homozygous	112671896
15	33160577	33160578	T	C	59	GENIC	homozygous	112671898
15	33161723	33161724	A	G	38	GENIC	homozygous	112671900
15	33161756	33161757	G	A	33	GENIC	homozygous	112671902
15	33161833	33161834	C	A	51	GENIC	homozygous	112671904
15	33164899	33164899		AGAA	43	GENIC	homozygous	131159164
15	33165247	33165248	C	T	34	GENIC	homozygous	112671906