chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	68177985	68177986	T	C	24	GENIC	possibly homozygous	117081906
10	68178502	68178503	T	C	20	GENIC	homozygous	117081908
10	68179235	68179236	G	A	25	GENIC	homozygous	117081910
10	68179450	68179451	T	C	28	GENIC	homozygous	116621338
10	68181163	68181164	C	T	23	GENIC	homozygous	117081912
10	68181510	68181511	C	G	27	GENIC	possibly homozygous	117104411
10	68181526	68181527	G	C	27	GENIC	heterozygous	118116027
10	68181822	68181823	C	T	28	GENIC	homozygous	117081914
10	68181856	68181857	C	T	37	GENIC	homozygous	117081916
10	68182146	68182147	C	T	13	GENIC	homozygous	117081918
10	68183071	68183072	A	T	17	GENIC	homozygous	118116028