chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	97815460	97815461	C	A	28	GENIC	possibly homozygous	67483039
13	97815764	97815765	C	A	23	GENIC	possibly homozygous	67483042
13	97815807	97815808	G	A	23	GENIC	possibly homozygous	67483045
13	97821257	97821258	T	A	21	GENIC	homozygous	67644113
13	97821299	97821300	T	A	25	GENIC	homozygous	67670565
13	97821308	97821309	A	C	27	GENIC	homozygous	67670567
13	97821207	97821208	T	C	30	GENIC	possibly homozygous	83573715
13	97821210	97821211	T	C	26	GENIC	homozygous	83573716
13	97821212	97821213	C	A	25	GENIC	possibly homozygous	83573717
13	97821215	97821216	A	G	27	GENIC	possibly homozygous	83573718
13	97822965	97822966	G	A	11	GENIC	possibly homozygous	67483051
13	97827349	97827350	T	C	20	GENIC	homozygous	67126429
13	97832896	97832897	G	A	15	GENIC	homozygous	67483063
13	97833632	97833633	A	G	29	GENIC	heterozygous	67644125
13	97832442	97832443	C	G	24	GENIC	homozygous	66376195