chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	91802655	91802656	T		53	GENIC	homozygous	137696947
6	91803029	91803030	T	C	52	GENIC	homozygous	141847466
6	91803486	91803487	G	T	47	GENIC	homozygous	141847467
6	91807178	91807179	A	G	43	GENIC	homozygous	141847468
6	91807373	91807374	C	T	51	GENIC	homozygous	141847469
6	91808651	91808652	T		34	GENIC	possibly homozygous	137696949
6	91809463	91809464	T		35	GENIC	homozygous	137696950
6	91810189	91810190	A	C	13	GENIC	homozygous	141847470
6	91814260	91814261	C	G	43	GENIC	possibly homozygous	141847471
6	91814505	91814506	C	T	50	GENIC	homozygous	141847472
6	91814263	91814275	CCCAAGCAGCGA		42	GENIC	possibly homozygous	141784070