chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	50299340	50299341	C	CT	16	GENIC	possibly homozygous	51004661
11	50299480	50299481	A	G	19	GENIC	homozygous	51004662
11	50299737	50299738	G	GCA	22	GENIC	homozygous	51357571
11	50300744	50300745	C	T	16	GENIC	homozygous	51357573
11	50301067	50301068	A	G	16	GENIC	homozygous	51004664
11	50301472	50301473	T	TAAA	8	GENIC	homozygous	51357575
11	50301756	50301757	T	TA	20	GENIC	heterozygous	51004667
11	50301756	50301757	T	TAA	20	GENIC	possibly homozygous	51201763
11	50302383	50302386	TTT	---	23	GENIC	possibly homozygous	51196007
11	50302384	50302386	TT	--	23	GENIC	heterozygous	51196008