chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208171009	208171010	T	-	4	GENIC	homozygous	59357325
2	208172508	208172509	A	G	13	GENIC	possibly homozygous	59357327
2	208172759	208172760	T	C	21	GENIC	homozygous	59357328
2	208173271	208173272	G	A	11	GENIC	homozygous	60301277
2	208173296	208173298	AA	--	1	GENIC	homozygous	59357329
2	208173601	208173602	C	A	3	GENIC	heterozygous	59357331
2	208175551	208175552	C	T	22	GENIC	possibly homozygous	59357338
2	208175763	208175764	C	T	16	GENIC	homozygous	60158843
2	208175980	208175981	T	C	12	GENIC	possibly homozygous	59357339
2	208176342	208176343	T	G	20	GENIC	homozygous	59932069
2	208177512	208177513	T	C	10	INTERGENIC	homozygous	59357341
2	208177782	208177783	T	TC	23	INTERGENIC	homozygous	59357342
2	208178859	208178860	C	T	24	GENIC	possibly homozygous	59357343
2	208178906	208178907	G	T	16	GENIC	homozygous	59357344
2	208179011	208179012	G	A	25	GENIC	homozygous	59357345
2	208179778	208179779	G	A	22	GENIC	possibly homozygous	59357347
2	208179871	208179872	A	G	20	GENIC	homozygous	59357348
2	208179935	208179936	A	G	25	GENIC	homozygous	59357349
2	208182450	208182451	G	T	1	GENIC	homozygous	59357351
2	208183091	208183092	A	G	2	GENIC	homozygous	59357354
2	208183134	208183135	C	CGG	2	GENIC	homozygous	59357355
2	208183200	208183201	A	C	15	GENIC	homozygous	59357356
2	208183390	208183391	A	G	8	GENIC	homozygous	59357357
2	208184112	208184113	C	CCTGGGT	2	GENIC	homozygous	59357362
2	208184783	208184784	G	A	16	GENIC	possibly homozygous	59357363
2	208185690	208185691	C	T	22	GENIC	possibly homozygous	59357364
2	208185769	208185770	A	G	25	GENIC	homozygous	59357365
2	208185966	208185975	CCTGCGAGG	---------	3	GENIC	heterozygous	59932072
2	208183382	208183383	G	A	11	GENIC	possibly homozygous	60456720
2	208183381	208183382	A	G	11	GENIC	possibly homozygous	60456719