chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	97446141	97446142	C	T	24	GENIC	homozygous	116592298
8	97446849	97446850	T	C	29	GENIC	homozygous	116855367
8	97447161	97447162	C	T	23	GENIC	homozygous	116855368
8	97450523	97450524	G	A	24	GENIC	homozygous	116592302
8	97452880	97452881	G	A	29	GENIC	homozygous	116855370
8	97452930	97452931	G	C	26	GENIC	homozygous	116855371
8	97453194	97453195	G	T	27	GENIC	homozygous	116855372
8	97454242	97454243	A	G	22	GENIC	homozygous	116592308
8	97457524	97457525	G	A	28	GENIC	homozygous	116855374
8	97457852	97457853	C	G	19	GENIC	homozygous	116592310
8	97458028	97458029	C	T	12	GENIC	homozygous	116855375