chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50537009	50537010	G	A	42	GENIC	homozygous	116815611
8	50537045	50537046	G	A	48	GENIC	homozygous	116815613
8	50537716	50537726	ATGGTCAAAT		40	GENIC	homozygous	130361747
8	50538082	50538083	G	T	13	GENIC	homozygous	117997048
8	50538172	50538173	T	C	38	GENIC	homozygous	116815615
8	50538343	50538344	G	A	46	GENIC	homozygous	117916785
8	50538086	50538087	A		16	GENIC	homozygous	128589259
8	50538243	50538243		C	50	GENIC	homozygous	128589262
8	50538345	50538345		G	47	GENIC	homozygous	128589264
8	50538156	50538156		G	33	GENIC	homozygous	128589260
8	50538187	50538188	C		39	GENIC	homozygous	128589261
8	50538340	50538341	G		45	GENIC	homozygous	128589263
8	50538245	50538246	A	C	50	GENIC	homozygous	116490280
8	50538357	50538358	G		44	GENIC	homozygous	128589265
8	50538358	50538359	G	C	45	GENIC	homozygous	117916786
8	50538360	50538361	G		46	GENIC	homozygous	128589266
8	50538365	50538366	A	G	50	GENIC	homozygous	117916787
8	50538369	50538370	G	A	52	GENIC	homozygous	117916788
8	50538369	50538369		AC	50	GENIC	homozygous	128589267
8	50538374	50538377	CCC		52	GENIC	homozygous	128589268
8	50538377	50538378	C	G	52	GENIC	homozygous	117916789
8	50538385	50538386	T		51	GENIC	homozygous	128589269
8	50538388	50538389	A		53	GENIC	homozygous	128589270
8	50538392	50538393	A		54	GENIC	homozygous	128589271