chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	97446141	97446142	C	T	53	GENIC	homozygous	116592298
8	97446849	97446850	T	C	41	GENIC	homozygous	116855367
8	97447161	97447162	C	T	54	GENIC	homozygous	116855368
8	97447373	97447374	G	C	39	GENIC	homozygous	116855369
8	97447924	97447925	T	C	24	GENIC	homozygous	116592300
8	97450523	97450524	G	A	51	GENIC	homozygous	116592302
8	97451807	97451807		G	39	GENIC	homozygous	128618789
8	97452695	97452695		CAACCACAGACCAAA	65	GENIC	homozygous	128618790
8	97452880	97452881	G	A	50	GENIC	homozygous	116855370
8	97452930	97452931	G	C	44	GENIC	homozygous	116855371
8	97453194	97453195	G	T	43	GENIC	homozygous	116855372
8	97454242	97454243	A	G	59	GENIC	homozygous	116592308
8	97455868	97455869	T		37	GENIC	homozygous	128618791
8	97456680	97456681	T		37	GENIC	homozygous	128618792
8	97457524	97457525	G	A	48	GENIC	homozygous	116855374
8	97457852	97457853	C	G	62	GENIC	homozygous	116592310
8	97458028	97458029	C	T	43	GENIC	homozygous	116855375
8	97456055	97456055		T	42	GENIC	homozygous	133193318