chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	50378113	50378114	G	A	41	GENIC	homozygous	114797138
6	50379901	50379902	G	A	45	GENIC	homozygous	114797139
6	50380399	50380400	G	T	36	GENIC	homozygous	114797140
6	50380679	50380680	T	C	44	GENIC	homozygous	114797141
6	50381206	50381207	A	G	58	GENIC	homozygous	114797142
6	50381517	50381518	T	A	65	GENIC	homozygous	114797143
6	50381591	50381592	A	G	80	GENIC	homozygous	114797144
6	50381624	50381625	T	A	80	GENIC	possibly homozygous	114797145
6	50382736	50382737	C	G	49	GENIC	possibly homozygous	114797146
6	50383265	50383266	C	A	41	GENIC	possibly homozygous	114797147
6	50383712	50383713	G	A	51	GENIC	homozygous	114797148
6	50383763	50383764	G	T	67	GENIC	possibly homozygous	114797149
6	50384111	50384112	T	C	42	GENIC	possibly homozygous	114797150
6	50384414	50384415	C	A	66	GENIC	homozygous	114797151
6	50384940	50384941	T	C	66	GENIC	homozygous	114797152
6	50385042	50385043	C	T	48	GENIC	homozygous	114797153
6	50385071	50385072	A	G	47	GENIC	homozygous	114797154
6	50385527	50385528	T	C	59	GENIC	homozygous	114797155
6	50385647	50385648	G	A	47	GENIC	homozygous	114797156
6	50386112	50386113	A	G	59	GENIC	homozygous	114797157
6	50386841	50386842	A	G	44	GENIC	homozygous	114797158
6	50386910	50386911	G	A	53	GENIC	homozygous	114797159
6	50387011	50387012	T	C	38	GENIC	homozygous	114797160
6	50387110	50387111	C	T	41	GENIC	homozygous	114797161
6	50387236	50387237	C	T	49	GENIC	homozygous	114797162
6	50387692	50387693	A	G	53	GENIC	homozygous	114797163
6	50388048	50388049	C	T	13	GENIC	homozygous	114797164