chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	99800538	99800539	A	G	44	GENIC	homozygous	144086862
10	99800543	99800544	T	C	45	GENIC	homozygous	144086863
10	99801005	99801005		CT	40	GENIC	homozygous	142207191
10	99802125	99802126	G	A	54	GENIC	homozygous	144086864
10	99802607	99802608	T	A	46	GENIC	homozygous	144086865
10	99805250	99805251	A	G	37	GENIC	homozygous	142263457
10	99811614	99811615	A	G	53	GENIC	homozygous	142263465
10	99813180	99813181	G	A	52	GENIC	homozygous	144086866
10	99814426	99814427	A	G	57	GENIC	homozygous	142263471
10	99817239	99817240	T	C	45	GENIC	homozygous	144086867
10	99817805	99817806	A	G	50	GENIC	homozygous	142263476
10	99819844	99819845	G	A	52	GENIC	homozygous	142263478
10	99820273	99820274	A	G	44	GENIC	homozygous	142263479
10	99820846	99820847	G	A	67	GENIC	homozygous	144086868
10	99803039	99803040	G		39	GENIC	possibly homozygous	144079249
10	99806809	99806809		GTAT	39	GENIC	homozygous	144079250
10	99822532	99822544	GGCTCGTGGGTA		44	GENIC	homozygous	144079251
10	99822863	99822864	C	G	37	GENIC	homozygous	142263480
10	99822925	99822925		TC	41	GENIC	homozygous	142207201
10	99823044	99823045	A	C	39	GENIC	possibly homozygous	144086869
10	99823810	99823811	A	G	48	GENIC	homozygous	142263482
10	99823832	99823833	G	A	47	GENIC	homozygous	144086870
10	99824155	99824156	T	C	43	GENIC	homozygous	144086871
10	99824389	99824389		C	9	GENIC	homozygous	142207202
10	99824426	99824427	C	T	15	GENIC	homozygous	144086872
10	99825306	99825307	G	A	53	GENIC	homozygous	144086873
10	99826497	99826498	C	T	53	GENIC	homozygous	142263483
10	99822648	99822649	C	T	24	GENIC	homozygous	403901706
10	99823442	99823443	A	C	26	GENIC	heterozygous	403296525
10	99822645	99822646	T	C	24	GENIC	homozygous	403901705