chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	250762815	250762816	A	G	19	GENIC	homozygous	74535878
2	250763598	250763599	T	C	13	GENIC	homozygous	75321283
2	250766307	250766308	A	T	35	GENIC	homozygous	74535884
2	250766430	250766431	G	A	29	GENIC	homozygous	75321284
2	250766441	250766442	G	A	34	GENIC	homozygous	74535887
2	250768610	250768611	C	T	26	GENIC	homozygous	74535893
2	250768931	250768932	C	T	39	GENIC	homozygous	75321285
2	250769401	250769402	G	A	33	GENIC	homozygous	75321286
2	250770530	250770531	G	C	17	GENIC	homozygous	75321287
2	250773408	250773409	T	C	32	GENIC	homozygous	75321290
2	250772071	250772072	T	G	16	GENIC	homozygous	75321288
2	250773227	250773228	C	T	26	GENIC	homozygous	75321289
2	250776655	250776656	C	G	43	GENIC	homozygous	75321291
2	250778011	250778012	G	A	20	GENIC	homozygous	75321292
2	250778149	250778150	C	T	36	GENIC	homozygous	75321293
2	250778374	250778375	G	A	24	GENIC	homozygous	75321294
2	250778709	250778710	A	G	10	GENIC	homozygous	75321295
2	250779015	250779016	A	T	18	GENIC	homozygous	75321297
2	250779856	250779857	G	A	27	GENIC	homozygous	74535914
2	250780188	250780189	G	A	34	GENIC	homozygous	75321298
2	250780207	250780208	T	G	32	GENIC	homozygous	74535917
2	250782306	250782307	G	A	26	GENIC	homozygous	75321300
2	250783670	250783671	C	T	28	GENIC	possibly homozygous	75321301