chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	21602509	21602510	C	T	46	GENIC	homozygous	111504119
3	21602585	21602586	G	A	52	GENIC	heterozygous	127977427
3	21602606	21602607	C	A	60	GENIC	heterozygous	111894917
3	21602626	21602627	G	T	59	GENIC	heterozygous	127977428
3	21603156	21603157	A	G	41	GENIC	homozygous	111504121
3	21603504	21603505	G	A	49	GENIC	homozygous	111504123
3	21604721	21604722	A	C	45	GENIC	heterozygous	111504125
3	21604737	21604738	T	G	43	GENIC	heterozygous	111504127
3	21604754	21604755	A	T	45	GENIC	heterozygous	111504128
3	21604846	21604847	A	G	45	GENIC	homozygous	111504132
3	21605050	21605051	A	G	48	GENIC	homozygous	111504134
3	21605076	21605077	G	T	61	GENIC	possibly homozygous	111504135
3	21605481	21605482	T	C	63	GENIC	possibly homozygous	111504137
3	21605495	21605496	T	C	62	GENIC	possibly homozygous	111504139
3	21605496	21605497	G	A	63	GENIC	possibly homozygous	111504141
3	21605526	21605527	C	A	53	GENIC	possibly homozygous	111504142
3	21606092	21606093	G	T	52	GENIC	possibly homozygous	111504144
3	21606313	21606314	A	G	58	GENIC	homozygous	111504146
3	21606825	21606826	A	G	60	GENIC	homozygous	111504148
3	21607850	21607851	A	G	55	GENIC	homozygous	111504150
3	21608616	21608617	G	C	55	GENIC	heterozygous	127977430
3	21608875	21608876	G	A	73	GENIC	heterozygous	112094863
3	21609467	21609468	T	C	34	GENIC	homozygous	111504152
3	21608621	21608624	AAT		54	GENIC	heterozygous	127859481
3	21602634	21602634		A	60	GENIC	heterozygous	127859479
3	21606072	21606075	TCT		49	GENIC	possibly homozygous	127859480