chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	142502535	142502536	G	A	22	GENIC	homozygous	59870378
2	142502778	142502779	A	C	22	GENIC	homozygous	59870379
2	142503235	142503236	T	TG	25	GENIC	homozygous	59870380
2	142504354	142504355	G	A	31	GENIC	homozygous	59870381
2	142505369	142505370	C	G	42	GENIC	possibly homozygous	59870382
2	142506503	142506504	T	C	32	GENIC	homozygous	59870383
2	142506688	142506689	A	G	20	GENIC	possibly homozygous	59870384
2	142506765	142506766	G	A	31	GENIC	homozygous	59870385
2	142507146	142507147	T	A	20	GENIC	possibly homozygous	59870386
2	142507395	142507396	G	GGACTGATGGGGGAGGTGGGCGA	31	GENIC	homozygous	60450979
2	142507580	142507581	T	C	29	GENIC	homozygous	59870388
2	142508985	142508986	C	G	10	GENIC	homozygous	59870389
2	142509082	142509083	T	C	10	GENIC	homozygous	59870390
2	142509466	142509467	C	T	21	GENIC	possibly homozygous	59870391
2	142509737	142509738	T	C	34	GENIC	possibly homozygous	59870392