chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	150685448	150685449	T	C	13	GENIC	homozygous	114540336
5	150685716	150685717	T	C	9	GENIC	homozygous	114348914
5	150686020	150686021	G	A	15	GENIC	homozygous	114540342
5	150686369	150686370	C	T	10	GENIC	homozygous	119183893
5	150686423	150686424	T	C	10	GENIC	homozygous	114540346
5	150686627	150686628	G	A	15	GENIC	homozygous	114540348
5	150687272	150687273	C	T	18	GENIC	homozygous	114348918
5	150687321	150687322	G	A	16	GENIC	possibly homozygous	114540352
5	150690906	150690907	T	C	14	GENIC	homozygous	114348924
5	150691762	150691763	G	T	13	GENIC	homozygous	114540370
5	150691895	150691896	C	T	9	GENIC	homozygous	114540372
5	150692007	150692008	G	A	7	GENIC	homozygous	114540374
5	150694736	150694737	T	C	7	GENIC	homozygous	114540378
5	150695315	150695316	C	G	17	GENIC	homozygous	114540380
5	150695753	150695754	G	A	17	GENIC	homozygous	114540382
5	150695760	150695761	C	T	17	GENIC	homozygous	114348944
5	150696514	150696515	C	T	10	GENIC	homozygous	114540384
5	150697024	150697025	C	T	12	GENIC	homozygous	114540386
5	150697095	150697096	A	C	11	GENIC	homozygous	114540388
5	150698126	150698127	C	A	16	GENIC	homozygous	114540396
5	150698211	150698212	G	A	12	GENIC	homozygous	114540398
5	150698221	150698222	C	G	11	GENIC	homozygous	114540400
5	150700013	150700014	G	A	19	GENIC	homozygous	114540402
5	150701466	150701467	T	C	32	GENIC	homozygous	114348956
5	150703071	150703072	A	C	6	GENIC	homozygous	114348958
5	150697094	150697095	C	A	10	GENIC	homozygous	118983914