chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50537008	50537009	C	T	55	GENIC	homozygous	117962644
8	50537045	50537046	G	A	58	GENIC	homozygous	116815613
8	50537735	50537736	A		39	GENIC	homozygous	133559894
8	50538172	50538173	T	C	23	GENIC	homozygous	116815615
8	50538343	50538344	G	A	35	GENIC	homozygous	117916785
8	50538345	50538345		G	35	GENIC	homozygous	128589264
8	50537738	50537739	T	G	38	GENIC	homozygous	118097485
8	50538106	50538107	C	T	16	GENIC	homozygous	118097487
8	50538086	50538087	A		11	GENIC	homozygous	128589259
8	50538156	50538156		G	17	GENIC	homozygous	128589260
8	50538187	50538188	C		21	GENIC	homozygous	128589261
8	50538243	50538243		C	32	GENIC	homozygous	128589262
8	50538340	50538341	G		32	GENIC	homozygous	128589263
8	50538245	50538246	A	C	32	GENIC	homozygous	116490280
8	50538357	50538358	G		36	GENIC	homozygous	128589265
8	50538358	50538359	G	C	36	GENIC	homozygous	117916786
8	50538360	50538361	G		35	GENIC	homozygous	128589266
8	50538365	50538366	A	G	36	GENIC	homozygous	117916787
8	50538369	50538370	G	A	39	GENIC	homozygous	117916788
8	50538369	50538369		AC	34	GENIC	homozygous	128589267
8	50538374	50538377	CCC		39	GENIC	homozygous	128589268
8	50538377	50538378	C	G	41	GENIC	homozygous	117916789
8	50538385	50538386	T		41	GENIC	homozygous	128589269
8	50538388	50538389	A		40	GENIC	homozygous	128589270
8	50538392	50538393	A		43	GENIC	homozygous	128589271
8	50538668	50538669	C	T	46	GENIC	homozygous	118097489