chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	132828942	132828943	G	A	17	GENIC	homozygous	116905484
8	132829194	132829195	C	T	36	GENIC	homozygous	116905486
8	132831177	132831178	G	A	30	GENIC	homozygous	116905488
8	132832819	132832820	T	C	18	GENIC	homozygous	116730002
8	132835630	132835631	T	C	26	GENIC	homozygous	116730009
8	132835847	132835848	C	G	23	GENIC	homozygous	116905492
8	132835992	132835993	A	G	31	GENIC	homozygous	116905494
8	132836100	132836101	A	G	34	GENIC	homozygous	116905496
8	132836252	132836253	G	T	25	GENIC	homozygous	116730010
8	132836459	132836460	G	A	33	GENIC	homozygous	116905498
8	132836539	132836540	G	A	43	GENIC	homozygous	116905500
8	132836550	132836551	C	A	38	GENIC	homozygous	116905502
8	132836608	132836609	A	G	32	GENIC	homozygous	116905504
8	132836902	132836903	T	G	27	GENIC	homozygous	116905506
8	132837174	132837175	A	C	33	GENIC	homozygous	116905508
8	132837196	132837197	T	C	37	GENIC	homozygous	116905510
8	132838025	132838026	G	T	30	GENIC	homozygous	116905512
8	132838253	132838254	G	A	32	GENIC	homozygous	116905514
8	132838389	132838390	G	A	25	GENIC	homozygous	116905516
8	132838490	132838491	T	C	29	GENIC	homozygous	116905518
8	132838681	132838682	A	T	41	GENIC	homozygous	116905520
8	132839257	132839258	C	T	32	GENIC	homozygous	116905522
8	132839373	132839374	T	G	30	GENIC	homozygous	116730011
8	132839601	132839602	T	C	41	GENIC	homozygous	116905524
8	132840641	132840642	T	C	31	GENIC	homozygous	116905526