chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	90486986	90486987	G	A	23	GENIC	homozygous	51035439
11	90487712	90487722	ACACACACAC	----------	11	GENIC	homozygous	50863619
11	90488279	90488280	C	CA	6	GENIC	heterozygous	50863620
11	90488279	90488280	C	CAAA	6	GENIC	heterozygous	51035440
11	90488972	90488978	CTCTCT	------	7	GENIC	heterozygous	51197691
11	90489166	90489167	C	G	24	GENIC	homozygous	51035442
11	90489189	90489191	AC	--	15	GENIC	homozygous	51035443
11	90489320	90489321	C	G	18	GENIC	homozygous	50974787
11	90490316	90490317	G	A	28	GENIC	homozygous	50974788
11	90491277	90491278	A	AGAGTCTGAGAG	26	GENIC	homozygous	50863626
11	90493614	90493615	C	T	24	GENIC	homozygous	50974790
11	90494735	90494765	GAAGCTCCCCCTCCAGTCAGGCCCTGCTCT	------------------------------	4	GENIC	homozygous	51192901
11	90488528	90488529	G	A	15	GENIC	homozygous	51135197
11	90488659	90488665	CCTCTC	------	7	GENIC	homozygous	51135200
11	90493854	90493855	C	T	17	GENIC	homozygous	51135203
11	90488968	90488978	CTCTCTCTCT	----------	7	GENIC	possibly homozygous	51192899
11	90494729	90494731	CC	--	4	GENIC	homozygous	51192900
11	90495377	90495378	T	C	16	GENIC	homozygous	50863632
11	90496278	90496279	C	T	15	GENIC	homozygous	50974793
11	90496297	90496298	A	G	12	GENIC	homozygous	50974794