chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	91135674	91135675	G	A	49	GENIC	homozygous	50865134
11	91135791	91135792	A	G	30	GENIC	homozygous	50865135
11	91136600	91136601	G	T	30	GENIC	heterozygous	50993058
11	91139277	91139278	G	A	27	GENIC	homozygous	50865136
11	91139463	91139464	G	T	35	GENIC	homozygous	50865137
11	91139902	91139903	C	CT	28	GENIC	homozygous	50865138
11	91141000	91141001	C	CAGATAGCTACTGCTA	19	GENIC	homozygous	50865139
11	91141011	91141012	A	T	34	GENIC	heterozygous	50865140
11	91141843	91141844	T	A	19	GENIC	homozygous	50865142
11	91142599	91142600	G	C	15	GENIC	homozygous	50865143
11	91143787	91143788	C	A	41	GENIC	homozygous	50865145
11	91144130	91144136	ACCACC	------	33	GENIC	homozygous	50865146
11	91144135	91144136	C	CA	43	GENIC	heterozygous	50865147
11	91144390	91144391	A	G	23	GENIC	homozygous	50865148
11	91145110	91145111	G	-	18	GENIC	homozygous	50975196
11	91145117	91145118	G	GTGCGC	19	GENIC	possibly homozygous	50865150
11	91145268	91145269	G	GA	4	GENIC	homozygous	50865151
11	91145276	91145277	T	A	6	GENIC	homozygous	50865152
11	91145502	91145503	C	T	28	GENIC	homozygous	50865153
11	91146234	91146235	C	-	11	GENIC	homozygous	50865154
11	91146239	91146242	AAA	---	6	GENIC	heterozygous	50865155
11	91146240	91146242	AA	--	6	GENIC	heterozygous	50865156
11	91146286	91146287	C	A	19	GENIC	homozygous	50865157
11	91146295	91146296	A	C	19	GENIC	possibly homozygous	50898814