chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90836831	90836832	T	C	28	GENIC	homozygous	115015102
13	90837131	90837132	A	G	45	GENIC	homozygous	115015104
13	90837892	90837893	T	C	32	GENIC	homozygous	115015106
13	90838111	90838112	G	A	29	GENIC	homozygous	115015108
13	90839468	90839469	T	C	30	GENIC	homozygous	115015110
13	90839731	90839732	G	A	33	GENIC	homozygous	115015112
13	90839933	90839934	G	A	29	GENIC	homozygous	115015114
13	90840281	90840282	C	T	30	GENIC	homozygous	115015116
13	90840374	90840375	G	A	29	GENIC	homozygous	115015118
13	90840489	90840490	C	T	24	GENIC	homozygous	115015120
13	90842094	90842095	A	G	31	GENIC	homozygous	114575282
13	90842931	90842932	A	G	27	GENIC	homozygous	115015122
13	90842945	90842946	G	A	27	GENIC	homozygous	115015124
13	90843127	90843128	A	G	37	GENIC	homozygous	114575286