chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	221254844	221254845	G	A	42	GENIC	homozygous	109368177
1	221255106	221255107	G	A	39	GENIC	homozygous	109368179
1	221255138	221255139	G	A	40	GENIC	homozygous	109368180
1	221258695	221258696	A	G	32	GENIC	homozygous	108544181
1	221260231	221260232	T	C	41	GENIC	homozygous	108544187
1	221261019	221261020	G	T	36	GENIC	homozygous	108544193
1	221261473	221261474	T	C	35	GENIC	homozygous	108544195
1	221262666	221262667	C	G	20	GENIC	homozygous	108544201
1	221263247	221263248	A	G	33	GENIC	homozygous	109368182
1	221263279	221263280	C	T	33	GENIC	homozygous	108544206
1	221263389	221263390	T	C	33	GENIC	homozygous	108544208
1	221264513	221264514	T	C	38	GENIC	homozygous	108544210
1	221264792	221264793	C	A	20	GENIC	homozygous	108544212
1	221265287	221265288	A	G	26	GENIC	homozygous	108544216
1	221265295	221265296	A	G	25	GENIC	homozygous	108544218
1	221265693	221265694	G	A	36	GENIC	possibly homozygous	108544220
1	221265711	221265712	A	G	45	GENIC	homozygous	108544222
1	221265801	221265802	A	T	38	GENIC	possibly homozygous	108544224
1	221266098	221266099	T	C	16	GENIC	homozygous	108544226
1	221266177	221266178	T	C	32	GENIC	possibly homozygous	108544228
1	221266365	221266366	A	G	40	GENIC	homozygous	108544230
1	221266622	221266623	G	A	45	GENIC	homozygous	108544232
1	221266741	221266742	C	T	46	GENIC	homozygous	108544234
1	221267053	221267054	A	T	16	GENIC	homozygous	109368183
1	221268701	221268702	A	G	31	GENIC	homozygous	108544238