chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50537045	50537046	G	A	50	GENIC	homozygous	116815613
8	50538106	50538107	C	T	29	GENIC	homozygous	118097487
8	50538172	50538173	T	C	32	GENIC	homozygous	116815615
8	50538357	50538358	G		48	GENIC	homozygous	128589265
8	50538086	50538087	A		24	GENIC	homozygous	128589259
8	50538156	50538156		G	31	GENIC	homozygous	128589260
8	50538187	50538188	C		42	GENIC	homozygous	128589261
8	50538243	50538243		C	50	GENIC	homozygous	128589262
8	50538340	50538341	G		46	GENIC	homozygous	128589263
8	50538345	50538345		G	48	GENIC	homozygous	128589264
8	50538245	50538246	A	C	51	GENIC	homozygous	116490280
8	50538343	50538344	G	A	47	GENIC	homozygous	117916785
8	50538358	50538359	G	C	48	GENIC	homozygous	117916786
8	50538360	50538361	G		48	GENIC	homozygous	128589266
8	50538365	50538366	A	G	44	GENIC	homozygous	117916787
8	50538369	50538370	G	A	42	GENIC	homozygous	117916788
8	50538369	50538369		AC	42	GENIC	homozygous	128589267
8	50538374	50538377	CCC		41	GENIC	homozygous	128589268
8	50538377	50538378	C	G	40	GENIC	homozygous	117916789
8	50538385	50538386	T		41	GENIC	homozygous	128589269
8	50538388	50538389	A		41	GENIC	homozygous	128589270
8	50538392	50538393	A		43	GENIC	homozygous	128589271
8	50538656	50538657	C	T	46	GENIC	homozygous	117940895