chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	90775736	90775737	T	C	15	GENIC	homozygous	50864457
11	90776922	90776923	C	A	21	GENIC	homozygous	50864458
11	90777135	90777136	T	G	22	GENIC	homozygous	50864459
11	90777136	90777137	T	C	22	GENIC	homozygous	50864460
11	90778961	90778962	G	GA	6	GENIC	heterozygous	50975020
11	90779011	90779012	A	G	18	GENIC	homozygous	50864462
11	90779187	90779188	A	G	25	GENIC	homozygous	50975021
11	90779406	90779407	T	C	19	GENIC	homozygous	50975022
11	90782090	90782091	C	G	9	GENIC	homozygous	50975023
11	90782381	90782382	G	GA	22	GENIC	homozygous	50975024
11	90782579	90782580	A	AGTGTGTGT	7	GENIC	homozygous	50864469
11	90782702	90782703	T	A	21	GENIC	homozygous	50975025
11	90782711	90782712	T	TTTTA	11	GENIC	homozygous	50975026
11	90782727	90782728	T	C	19	GENIC	possibly homozygous	50975027
11	90782834	90782835	G	C	13	GENIC	homozygous	50864471
11	90782855	90782856	A	T	21	GENIC	homozygous	50975028
11	90782874	90782875	C	T	22	GENIC	homozygous	50975029
11	90783231	90783232	G	A	18	GENIC	homozygous	50975030
11	90783272	90783273	A	AT	18	GENIC	possibly homozygous	50864476
11	90783277	90783278	A	AG	17	GENIC	heterozygous	50864477
11	90783293	90783295	GC	--	19	GENIC	heterozygous	50864478
11	90783302	90783303	G	A	23	GENIC	homozygous	50864479
11	90783330	90783331	G	A	24	GENIC	homozygous	50975031
11	90784129	90784130	A	C	26	GENIC	homozygous	50975032
11	90785823	90785824	T	C	18	GENIC	homozygous	50864483