chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	283479779	283479780	C	A	26	GENIC	homozygous	59617363
2	283481899	283481903	AAGG	----	9	GENIC	homozygous	59617365
2	283481936	283481937	G	A	24	GENIC	homozygous	59617371
2	283483498	283483499	T	C	45	GENIC	homozygous	59617373
2	283483790	283483791	G	A	18	GENIC	homozygous	59617375
2	283483866	283483867	A	G	22	GENIC	homozygous	59617377
2	283484582	283484583	A	T	31	GENIC	homozygous	59617379
2	283484762	283484764	TA	--	33	GENIC	homozygous	59617381
2	283484878	283484879	A	G	40	GENIC	homozygous	59617383
2	283484958	283484959	C	-	30	GENIC	homozygous	59617385
2	283488430	283488431	T	C	34	GENIC	homozygous	59617387
2	283493307	283493311	AAAA	----	12	GENIC	homozygous	59617389
2	283493864	283493865	A	AT	15	GENIC	homozygous	59617393
2	283494030	283494031	G	GAAAAC	16	GENIC	homozygous	59617395
2	283494313	283494314	A	AT	23	GENIC	possibly homozygous	59617397
2	283497587	283497588	T	C	27	GENIC	homozygous	59617399
2	283497656	283497658	AA	--	23	GENIC	heterozygous	59617401
2	283497657	283497658	A	-	23	GENIC	possibly homozygous	59617403
2	283498119	283498120	A	T	14	GENIC	homozygous	59617407
2	283498827	283498828	T	C	26	GENIC	homozygous	59617409
2	283499132	283499134	AA	--	16	GENIC	homozygous	59782660
2	283501173	283501174	G	C	22	GENIC	homozygous	59617411
2	283501278	283501279	C	CTT	22	GENIC	homozygous	59617413
2	283503972	283503973	C	T	9	GENIC	homozygous	59617415