chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	211531304	211531306	GA		11	GENIC	homozygous	141337257
2	211532243	211532244	C	T	22	GENIC	homozygous	141436614
2	211532915	211532916	T	C	16	GENIC	homozygous	141436615
2	211532781	211532782	A	G	15	GENIC	homozygous	136459195
2	211533184	211533185	T	C	12	GENIC	homozygous	136459196
2	211534400	211534401	T	C	26	GENIC	homozygous	136459197
2	211535374	211535375	G	A	9	GENIC	homozygous	141436616
2	211537411	211537412	G	A	23	GENIC	homozygous	141436617
2	211537794	211537795	T	C	16	GENIC	homozygous	136459200
2	211537849	211537850	G	A	23	GENIC	homozygous	141436618
2	211537949	211537950	T	A	23	GENIC	homozygous	141436619
2	211538953	211538954	G	C	17	GENIC	homozygous	141436620
2	211539180	211539181	C	T	18	GENIC	homozygous	141436621
2	211539676	211539677	G	A	18	GENIC	homozygous	136459201
2	211541153	211541154	C	A	16	GENIC	homozygous	141436622
2	211541395	211541396	A		19	GENIC	possibly homozygous	141337258
2	211542282	211542283	C	A	8	GENIC	homozygous	141436623
2	211543727	211543728	A	G	27	GENIC	homozygous	141436624
2	211545663	211545663		TCC	15	GENIC	homozygous	141337259
2	211545723	211545724	T	G	16	GENIC	homozygous	136459202
2	211546780	211546781	A	G	12	GENIC	homozygous	141436625
2	211542330	211542331	C		12	GENIC	heterozygous	403038763
2	211542330	211542331	C	G	12	GENIC	homozygous	154049902
2	211540728	211540728		CACT	18	GENIC	homozygous	135977224