chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	40031103	40031104	T	C	10	GENIC	homozygous	51586237
11	40031821	40031822	C	T	18	GENIC	homozygous	50743737
11	40032607	40032608	G	A	20	GENIC	homozygous	50743739
11	40032858	40032859	T	G	21	GENIC	homozygous	51160796
11	40033361	40033362	A	G	22	GENIC	homozygous	50743740
11	40033501	40033502	T	C	10	GENIC	heterozygous	51066669
11	40033799	40033800	C	T	25	GENIC	homozygous	51586239
11	40036059	40036060	A	G	3	GENIC	homozygous	50743745
11	40036835	40036836	T	-	8	GENIC	heterozygous	51160797
11	40037241	40037242	C	G	23	GENIC	homozygous	51160798
11	40037438	40037439	C	CT	7	GENIC	heterozygous	50743747
11	40037617	40037618	T	C	15	GENIC	homozygous	51160799
11	40037745	40037746	T	TTC	5	GENIC	heterozygous	51586241
11	40037779	40037780	T	TTCCC	6	GENIC	homozygous	51586243
11	40039251	40039252	G	A	18	GENIC	homozygous	51160800
11	40039845	40039846	A	G	21	GENIC	possibly homozygous	51160801
11	40040083	40040084	G	A	17	GENIC	homozygous	51160802
11	40040843	40040844	G	A	20	GENIC	homozygous	51586245
11	40041119	40041120	C	T	26	GENIC	homozygous	51586247
11	40041523	40041524	G	A	26	GENIC	homozygous	51586249
11	40041748	40041749	A	G	25	GENIC	homozygous	51160803