chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	97439686	97439687	T	C	16	GENIC	homozygous	116592278
8	97439699	97439700	G	A	23	GENIC	homozygous	116592280
8	97441281	97441282	C	T	27	GENIC	homozygous	116592282
8	97441725	97441726	A	T	28	GENIC	homozygous	116592284
8	97442262	97442263	T	G	27	GENIC	homozygous	116592286
8	97443023	97443024	C	T	27	GENIC	homozygous	116592288
8	97443280	97443281	C	T	34	GENIC	homozygous	116592290
8	97443319	97443320	C	T	22	GENIC	homozygous	116592292
8	97443320	97443321	A	G	23	GENIC	homozygous	116592294
8	97445847	97445848	A	G	20	GENIC	homozygous	116592296
8	97446141	97446142	C	T	30	GENIC	homozygous	116592298
8	97450523	97450524	G	A	25	GENIC	homozygous	116592302
8	97450721	97450722	C	T	17	GENIC	homozygous	116592304
8	97451630	97451631	G	A	33	GENIC	homozygous	116592306
8	97454242	97454243	A	G	22	GENIC	homozygous	116592308
8	97457852	97457853	C	G	23	GENIC	homozygous	116592310