chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	50229727	50229728	T	TTTTTC	10	GENIC	homozygous	51004567
11	50229744	50229745	G	T	14	GENIC	homozygous	51357364
11	50229817	50229818	T	TTTTTTTG	18	GENIC	possibly homozygous	51357366
11	50231009	50231010	A	-	11	GENIC	heterozygous	51004569
11	50231118	50231119	C	T	38	GENIC	possibly homozygous	51357368
11	50231639	50231640	T	C	20	GENIC	homozygous	51004570
11	50231673	50231674	A	G	19	GENIC	homozygous	51357370
11	50231796	50231797	A	G	28	GENIC	homozygous	51004571
11	50232310	50232311	A	G	34	GENIC	homozygous	51357372
11	50233487	50233488	T	A	26	GENIC	possibly homozygous	51357374
11	50233888	50233889	A	-	30	GENIC	possibly homozygous	51288550
11	50234078	50234079	T	A	34	GENIC	possibly homozygous	51357376
11	50234237	50234238	C	T	21	GENIC	possibly homozygous	51357378