chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208171009	208171010	T	-	2	GENIC	homozygous	59357325
2	208172508	208172509	A	G	22	GENIC	homozygous	59357327
2	208172759	208172760	T	C	28	GENIC	homozygous	59357328
2	208173296	208173298	AA	--	2	GENIC	heterozygous	59357329
2	208173601	208173602	C	A	2	GENIC	heterozygous	59357331
2	208173619	208173620	G	A	2	GENIC	homozygous	59357332
2	208175127	208175128	G	GAGGC	5	GENIC	homozygous	59357337
2	208175551	208175552	C	T	21	GENIC	possibly homozygous	59357338
2	208175980	208175981	T	C	18	GENIC	homozygous	59357339
2	208177471	208177473	TC	--	2	INTERGENIC	heterozygous	59357340
2	208177512	208177513	T	C	15	INTERGENIC	homozygous	59357341
2	208177782	208177783	T	TC	19	INTERGENIC	homozygous	59357342
2	208178859	208178860	C	T	24	GENIC	possibly homozygous	59357343
2	208178906	208178907	G	T	17	GENIC	homozygous	59357344
2	208179011	208179012	G	A	21	GENIC	homozygous	59357345
2	208179128	208179129	T	TGGG	8	GENIC	heterozygous	59357346
2	208179129	208179130	T	G	8	GENIC	heterozygous	59771539
2	208179778	208179779	G	A	22	GENIC	homozygous	59357347
2	208179871	208179872	A	G	30	GENIC	homozygous	59357348
2	208179935	208179936	A	G	22	GENIC	homozygous	59357349
2	208182450	208182451	G	T	1	GENIC	homozygous	59357351
2	208182515	208182516	A	-	2	GENIC	heterozygous	59357352
2	208182537	208182538	A	-	1	GENIC	homozygous	59357353
2	208183091	208183092	A	G	4	GENIC	heterozygous	59357354
2	208183134	208183135	C	CGG	1	GENIC	homozygous	59357355
2	208183200	208183201	A	C	32	GENIC	possibly homozygous	59357356
2	208183381	208183382	A	G	5	GENIC	homozygous	60456719
2	208183382	208183383	G	A	5	GENIC	homozygous	60456720
2	208183390	208183391	A	G	11	GENIC	homozygous	59357357
2	208183858	208183859	A	T	2	GENIC	homozygous	59357361
2	208184112	208184113	C	CCTGGGT	4	GENIC	homozygous	59357362
2	208184783	208184784	G	A	23	GENIC	possibly homozygous	59357363
2	208185690	208185691	C	T	24	GENIC	possibly homozygous	59357364
2	208185769	208185770	A	G	22	GENIC	homozygous	59357365