chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	50299340	50299341	C	CT	13	GENIC	possibly homozygous	51004661
11	50299480	50299481	A	G	29	GENIC	homozygous	51004662
11	50299990	50299991	C	G	32	GENIC	homozygous	51004663
11	50301067	50301068	A	G	32	GENIC	homozygous	51004664
11	50301570	50301571	G	T	33	GENIC	homozygous	51004666
11	50301756	50301757	T	TA	25	GENIC	possibly homozygous	51004667
11	50301756	50301757	T	TAA	25	GENIC	heterozygous	51201763
11	50302384	50302386	TT	--	18	GENIC	homozygous	51196008
11	50302623	50302624	G	GT	28	GENIC	homozygous	51004669