chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	221274047	221274048	T	G	31	GENIC	homozygous	108544248
1	221274064	221274065	T	C	33	GENIC	homozygous	108544250
1	221274147	221274148	G	T	24	GENIC	homozygous	109368185
1	221274400	221274401	C	T	16	GENIC	homozygous	109368187
1	221274483	221274484	A	G	19	GENIC	homozygous	108544254
1	221274534	221274535	G	C	20	GENIC	homozygous	108544256
1	221274958	221274959	A	T	30	GENIC	homozygous	108544258
1	221275539	221275540	T	C	32	GENIC	homozygous	108544262
1	221275615	221275616	T	C	32	GENIC	homozygous	108544264
1	221275775	221275776	C	T	24	GENIC	possibly homozygous	108544266
1	221276196	221276197	T	C	33	GENIC	possibly homozygous	108544268
1	221276268	221276269	C	G	22	GENIC	homozygous	108544270
1	221276519	221276520	T	C	16	GENIC	homozygous	108544276
1	221276575	221276576	T	G	22	GENIC	homozygous	108544278
1	221276798	221276799	A	G	21	GENIC	homozygous	108544280
1	221276857	221276858	G	T	27	GENIC	homozygous	108544282
1	221277042	221277043	G	A	29	GENIC	homozygous	108544284
1	221278159	221278160	T	C	22	GENIC	homozygous	108544292
1	221278752	221278753	T	C	15	GENIC	homozygous	108544294
1	221278833	221278834	A	G	17	GENIC	homozygous	108544296
1	221279106	221279107	G	T	16	GENIC	homozygous	108544298
1	221279640	221279641	A	C	10	GENIC	homozygous	108544302
1	221280984	221280985	A	G	25	GENIC	homozygous	108544304