chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	50378113	50378114	G	A	14	GENIC	homozygous	114797138
6	50379901	50379902	G	A	19	GENIC	homozygous	114797139
6	50380679	50380680	T	C	21	GENIC	homozygous	114797141
6	50381206	50381207	A	G	21	GENIC	homozygous	114797142
6	50381517	50381518	T	A	23	GENIC	homozygous	114797143
6	50381591	50381592	A	G	19	GENIC	homozygous	114797144
6	50381624	50381625	T	A	17	GENIC	homozygous	114797145
6	50382736	50382737	C	G	25	GENIC	homozygous	114797146
6	50383265	50383266	C	A	30	GENIC	homozygous	114797147
6	50383712	50383713	G	A	20	GENIC	homozygous	114797148
6	50383763	50383764	G	T	26	GENIC	homozygous	114797149
6	50384111	50384112	T	C	21	GENIC	homozygous	114797150
6	50384414	50384415	C	A	27	GENIC	homozygous	114797151
6	50384940	50384941	T	C	16	GENIC	homozygous	114797152
6	50385042	50385043	C	T	19	GENIC	homozygous	114797153
6	50385071	50385072	A	G	18	GENIC	homozygous	114797154
6	50385527	50385528	T	C	22	GENIC	homozygous	114797155
6	50385647	50385648	G	A	28	GENIC	homozygous	114797156
6	50386112	50386113	A	G	31	GENIC	homozygous	114797157
6	50386841	50386842	A	G	39	GENIC	homozygous	114797158
6	50386910	50386911	G	A	28	GENIC	homozygous	114797159
6	50387011	50387012	T	C	22	GENIC	homozygous	114797160
6	50387110	50387111	C	T	15	GENIC	possibly homozygous	114797161
6	50387236	50387237	C	T	21	GENIC	homozygous	114797162
6	50387692	50387693	A	G	24	GENIC	homozygous	114797163
6	50388048	50388049	C	T	14	GENIC	homozygous	114797164