chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50537009	50537010	G	A	18	GENIC	homozygous	116815611
8	50537045	50537046	G	A	17	GENIC	homozygous	116815613
8	50537716	50537726	ATGGTCAAAT		16	GENIC	homozygous	130361747
8	50538082	50538083	G	T	10	GENIC	homozygous	117997048
8	50538086	50538087	A		11	GENIC	homozygous	128589259
8	50538156	50538156		G	10	GENIC	homozygous	128589260
8	50538172	50538173	T	C	10	GENIC	homozygous	116815615
8	50538187	50538188	C		10	GENIC	homozygous	128589261
8	50538243	50538243		C	15	GENIC	homozygous	128589262
8	50538340	50538341	G		15	GENIC	homozygous	128589263
8	50538343	50538344	G	A	14	GENIC	homozygous	117916785
8	50538345	50538345		G	14	GENIC	homozygous	128589264
8	50538357	50538358	G		13	GENIC	homozygous	128589265
8	50538358	50538359	G	C	13	GENIC	homozygous	117916786
8	50538360	50538361	G		13	GENIC	homozygous	128589266
8	50538365	50538366	A	G	12	GENIC	homozygous	117916787
8	50538369	50538370	G	A	13	GENIC	homozygous	117916788
8	50538369	50538369		AC	12	GENIC	homozygous	128589267
8	50538374	50538377	CCC		13	GENIC	homozygous	128589268
8	50538377	50538378	C	G	13	GENIC	homozygous	117916789
8	50538385	50538386	T		13	GENIC	homozygous	128589269
8	50538388	50538389	A		13	GENIC	homozygous	128589270
8	50538392	50538393	A		15	GENIC	homozygous	128589271
8	50538245	50538246	A	C	15	GENIC	homozygous	116490280