chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	51987724	51987725	A	G	19	GENIC	homozygous	114800275
6	51988602	51988603	G	A	28	GENIC	homozygous	114800276
6	51988771	51988772	T	C	24	GENIC	homozygous	114800277
6	51989048	51989049	C	A	13	GENIC	homozygous	114800278
6	51989738	51989739	A	G	38	GENIC	homozygous	114800279
6	51989752	51989753	A	G	35	GENIC	homozygous	114800280
6	51989909	51989910	T	A	38	GENIC	homozygous	114800281
6	51990285	51990286	C	G	31	GENIC	homozygous	114800282
6	51990452	51990453	T	C	25	GENIC	homozygous	114800283
6	51990606	51990607	T	G	34	GENIC	homozygous	114800284
6	51991121	51991122	G	A	25	GENIC	homozygous	114800285
6	51991463	51991464	A	T	10	GENIC	homozygous	114800286
6	51991813	51991814	A	G	19	GENIC	homozygous	114800287
6	51991841	51991842	C	T	24	GENIC	homozygous	114800288
6	51992023	51992024	G	A	22	GENIC	homozygous	114800289
6	51992676	51992677	G	T	25	GENIC	homozygous	114800290
6	51993777	51993778	C	A	22	GENIC	homozygous	114800291
6	51993802	51993803	C	T	26	GENIC	homozygous	114800292
6	51994009	51994010	A	C	31	GENIC	homozygous	114800293