chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82366865	82366865		A	59	GENIC	homozygous	128838162
10	82367073	82367074	A	G	60	GENIC	homozygous	116658521
10	82369250	82369251	T	C	70	GENIC	homozygous	116658523
10	82369523	82369524	A	G	50	GENIC	homozygous	116658525
10	82370235	82370236	T	C	57	GENIC	homozygous	116658529
10	82370448	82370449	T	C	69	GENIC	possibly homozygous	116658531
10	82370795	82370796	T	C	53	GENIC	homozygous	116658533
10	82371271	82371272	C	G	43	GENIC	homozygous	116658535
10	82371900	82371901	C	A	38	GENIC	homozygous	116658539
10	82371949	82371950	T	C	44	GENIC	homozygous	116658541
10	82371957	82371958	C	T	42	GENIC	homozygous	116658543
10	82372872	82372873	C	T	55	GENIC	homozygous	116658545
10	82368557	82368567	TGTGTCTGTC		36	GENIC	homozygous	131467521
10	82373306	82373307	C		47	GENIC	homozygous	131467522
10	82372926	82372927	C	T	52	GENIC	homozygous	117017827
10	82373315	82373316	A	G	44	GENIC	homozygous	117017828