chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	97349387	97349388	A	G	12	GENIC	homozygous	113933398
5	97349651	97349652	A	T	27	GENIC	homozygous	113933399
5	97349690	97349691	T	G	30	GENIC	homozygous	113933400
5	97351046	97351047	T	C	15	GENIC	homozygous	113933401
5	97351772	97351773	A	G	14	GENIC	possibly homozygous	113933402
5	97352256	97352257	A	T	14	GENIC	homozygous	113933403
5	97352315	97352316	C	T	14	GENIC	homozygous	113933404
5	97352549	97352550	A	G	15	GENIC	homozygous	113933405
5	97353039	97353040	G	T	16	GENIC	homozygous	113933407
5	97353364	97353365	C	T	15	GENIC	homozygous	113933408
5	97353417	97353418	T	G	19	GENIC	homozygous	113933409
5	97353581	97353582	C	T	13	GENIC	homozygous	113933410