chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	38064035	38064036	A	G	30	GENIC	homozygous	116129776
11	38064173	38064174	T	G	20	GENIC	homozygous	116129778
11	38064219	38064220	A	G	16	GENIC	homozygous	116129780
11	38064245	38064246	A		16	GENIC	homozygous	131716405
11	38064569	38064570	T	A	20	GENIC	homozygous	116129782
11	38064604	38064605	T	C	20	GENIC	homozygous	116129784
11	38064751	38064752	A	G	26	GENIC	homozygous	116129786
11	38065532	38065533	A	G	23	GENIC	homozygous	116129788
11	38065536	38065536		CA	23	GENIC	homozygous	131716406
11	38066069	38066070	A	G	23	GENIC	homozygous	116129790
11	38066180	38066181	C	T	20	GENIC	homozygous	116129792
11	38066338	38066339	A	C	21	GENIC	homozygous	116129794
11	38067423	38067424	A	G	27	GENIC	homozygous	116129796
11	38067657	38067658	T	C	30	GENIC	homozygous	116129798
11	38070502	38070503	T	A	17	GENIC	possibly homozygous	116129800
11	38070601	38070609	AGAGAGAC		9	GENIC	possibly homozygous	131716407
11	38067305	38067306	T	C	20	GENIC	homozygous	115832857
11	38067671	38067672	T	G	29	GENIC	homozygous	115832859