chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82770963	82770964	C	T	56	GENIC	possibly homozygous	116898434
10	82771428	82771429	G	C	62	GENIC	homozygous	116898435
10	82771589	82771589		AG	44	GENIC	homozygous	128838538
10	82772237	82772238	G	A	41	GENIC	homozygous	116898437
10	82773068	82773069	A	G	52	GENIC	homozygous	116898439
10	82773159	82773160	A	G	56	GENIC	homozygous	116659752
10	82771684	82771685	C	T	49	GENIC	homozygous	116659746
10	82772620	82772621	A	T	56	GENIC	homozygous	116659748
10	82773090	82773091	C	T	56	GENIC	homozygous	116659750
10	82773170	82773171	T	C	58	GENIC	homozygous	116659754
10	82773191	82773191		CTGAGCAC	55	GENIC	homozygous	128838539
10	82773397	82773398	A	G	43	GENIC	homozygous	116898441
10	82774333	82774334	C	T	44	GENIC	homozygous	116898449
10	82774344	82774344		T	45	GENIC	homozygous	128838543
10	82774346	82774347	A		45	GENIC	homozygous	128838544
10	82774348	82774349	T	A	45	GENIC	homozygous	116980607
10	82774352	82774353	C	T	44	GENIC	homozygous	117144287
10	82774353	82774354	A	G	46	GENIC	homozygous	116659756
10	82774356	82774357	G	A	45	GENIC	homozygous	117144289
10	82774359	82774360	A	G	45	GENIC	homozygous	117144291
10	82782215	82782216	G	A	51	GENIC	homozygous	116898451
10	82782260	82782261	C	T	39	GENIC	homozygous	116898453
10	82782797	82782798	C		16	GENIC	homozygous	128838545
10	82782804	82782804		C	15	GENIC	homozygous	128838546
10	82783839	82783840	T	C	42	GENIC	homozygous	116898455
10	82784338	82784339	C	T	48	GENIC	homozygous	117144293
10	82784522	82784523	T	G	46	GENIC	possibly homozygous	117144295
10	82776820	82776820		AA	25	GENIC	homozygous	132146742
10	82784699	82784699		TGC	57	GENIC	homozygous	132146743