chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82367073	82367074	A	G	56	GENIC	homozygous	116658521
10	82368590	82368591	C	G	48	GENIC	possibly homozygous	117391840
10	82369250	82369251	T	C	47	GENIC	homozygous	116658523
10	82369523	82369524	A	G	48	GENIC	homozygous	116658525
10	82369815	82369816	C	T	67	GENIC	homozygous	116658527
10	82370235	82370236	T	C	52	GENIC	homozygous	116658529
10	82370448	82370449	T	C	53	GENIC	homozygous	116658531
10	82370795	82370796	T	C	72	GENIC	homozygous	116658533
10	82371271	82371272	C	G	63	GENIC	homozygous	116658535
10	82371717	82371718	A	G	51	GENIC	homozygous	116658537
10	82371900	82371901	C	A	42	GENIC	possibly homozygous	116658539
10	82371949	82371950	T	C	56	GENIC	homozygous	116658541
10	82371957	82371958	C	T	60	GENIC	homozygous	116658543
10	82372872	82372873	C	T	63	GENIC	homozygous	116658545
10	82375305	82375306	T	A	33	GENIC	homozygous	118046403
10	82373716	82373717	C	T	65	GENIC	homozygous	118046400
10	82374069	82374070	G	A	65	GENIC	homozygous	118046401
10	82374735	82374736	T	C	70	GENIC	possibly homozygous	118046402