chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	69721275	69721276	C	T	27	GENIC	homozygous	54895984
6	69722728	69722729	A	G	21	GENIC	homozygous	54487138
6	69723866	69723867	G	GAA	26	GENIC	heterozygous	54487142
6	69723866	69723867	G	GA	26	GENIC	heterozygous	54487144
6	69724576	69724577	G	C	26	GENIC	homozygous	54487148
6	69724905	69724906	C	T	43	GENIC	homozygous	54487154
6	69725373	69725375	AA	--	23	GENIC	possibly homozygous	55074108
6	69726623	69726624	A	ACAGTCAC	21	GENIC	homozygous	54487167
6	69727900	69727901	C	T	38	GENIC	homozygous	54487185
6	69728236	69728237	C	CT	30	GENIC	homozygous	54487189
6	69729985	69729986	C	-	25	GENIC	homozygous	54895988
6	69730061	69730062	A	-	38	GENIC	homozygous	54895990
6	69730608	69730609	C	A	25	GENIC	homozygous	54895992
6	69731518	69731520	AG	--	27	GENIC	homozygous	54487207
6	69732204	69732205	G	T	28	GENIC	possibly homozygous	54895994
6	69733117	69733118	C	CTTA	35	GENIC	homozygous	54487209
6	69733241	69733242	G	A	25	GENIC	homozygous	54895995
6	69734408	69734409	T	G	26	GENIC	homozygous	54895999
6	69736346	69736347	A	-	25	GENIC	homozygous	54896001
6	69737720	69737721	T	TG	23	GENIC	homozygous	54487223
6	69738940	69738941	A	G	14	GENIC	homozygous	54487225