chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	77102288	77102289	G	A	22	GENIC	homozygous	51590165
11	77102507	77102508	G	A	32	GENIC	possibly homozygous	51223473
11	77102534	77102535	T	G	29	GENIC	possibly homozygous	51223475
11	77102863	77102864	C	T	57	GENIC	homozygous	51590167
11	77103008	77103009	T	C	35	GENIC	homozygous	51590169
11	77103184	77103185	C	CG	26	GENIC	homozygous	51048847
11	77102995	77102999	ATGT	----	36	GENIC	homozygous	51048845
11	77103216	77103217	C	T	29	GENIC	homozygous	51590171
11	77103354	77103355	C	T	28	GENIC	homozygous	51590173
11	77103717	77103718	T	C	25	GENIC	possibly homozygous	51048850
11	77103820	77103821	G	T	25	GENIC	homozygous	51590175
11	77103931	77103933	AC	--	19	GENIC	possibly homozygous	51590177
11	77104005	77104006	A	T	37	GENIC	homozygous	51048852
11	77104340	77104341	T	-	20	GENIC	homozygous	51590178
11	77104357	77104358	C	T	16	GENIC	homozygous	51048863
11	77104458	77104459	G	A	31	GENIC	homozygous	51590181
11	77104499	77104500	T	C	31	GENIC	homozygous	51048865
11	77104575	77104576	G	A	26	GENIC	homozygous	51590183
11	77104762	77104763	T	TG	36	GENIC	homozygous	51048866
11	77104906	77104907	T	G	25	GENIC	homozygous	51590185
11	77104919	77104920	T	C	27	GENIC	homozygous	51048868
11	77104966	77104967	A	G	33	GENIC	homozygous	51048870
11	77105881	77105882	G	A	28	GENIC	homozygous	51223488
11	77105994	77105995	A	G	30	GENIC	homozygous	51590187
11	77106067	77106068	G	A	23	GENIC	homozygous	51223490
11	77106167	77106168	A	G	30	GENIC	homozygous	51223492
11	77107106	77107107	A	G	25	GENIC	homozygous	51590189
11	77107254	77107255	G	C	36	GENIC	homozygous	51048880
11	77107454	77107455	A	G	23	GENIC	homozygous	51048882
11	77107645	77107646	C	T	20	GENIC	homozygous	51048884
11	77107691	77107692	G	A	26	GENIC	homozygous	51223494
11	77107867	77107868	C	T	29	GENIC	homozygous	51223496
11	77107974	77107975	C	T	25	GENIC	homozygous	51048886
11	77108287	77108288	G	A	29	GENIC	homozygous	51590191
11	77108750	77108751	C	T	29	GENIC	homozygous	51590193
11	77109506	77109507	C	T	38	GENIC	homozygous	51223499
11	77109684	77109685	C	T	39	GENIC	possibly homozygous	51223501
11	77109859	77109860	T	C	35	GENIC	homozygous	51048890
11	77109921	77109922	C	CACATAT	28	GENIC	possibly homozygous	51048891
11	77109944	77109946	AT	--	30	GENIC	possibly homozygous	51223503
11	77109980	77109981	T	TACGCACATACAC	37	GENIC	possibly homozygous	51189876
11	77109986	77109987	C	T	33	GENIC	possibly homozygous	51048896
11	77110110	77110111	T	TATATACAC	2	GENIC	heterozygous	51223505
11	77110171	77110172	G	A	26	GENIC	homozygous	51223507
11	77110224	77110230	ATATAC	------	25	GENIC	possibly homozygous	51223509
11	77110437	77110439	AA	--	20	GENIC	homozygous	51223511
11	77110555	77110673	AAGCTAGTTGCTGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGATCCCCAACTCCGAAAAAAAGAACCGGGGGGGGGGGGGGGGGGG	----------------------------------------------------------------------------------------------------------------------	23	GENIC	homozygous	51189884
11	77111170	77111171	A	C	30	GENIC	homozygous	51048912
11	77112412	77112413	C	G	34	GENIC	homozygous	51048914
11	77112514	77112515	G	C	38	GENIC	homozygous	51048916
11	77112573	77112574	C	T	31	GENIC	homozygous	51223515
11	77112997	77112998	A	AAGAC	18	GENIC	homozygous	51590194