chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	73026732	73026733	T	C	22	GENIC	homozygous	109828518
2	73026783	73026784	A	G	29	GENIC	homozygous	109828519
2	73026786	73026787	A	G	26	GENIC	homozygous	110936342
2	73027051	73027052	T	G	3	GENIC	homozygous	109828521
2	73027062	73027063	T	C	6	GENIC	heterozygous	120389090
2	73027982	73027983	T	C	19	GENIC	homozygous	109828522
2	73028015	73028016	T	C	22	GENIC	homozygous	109828523
2	73028068	73028069	T	C	25	GENIC	homozygous	110936344
2	73028272	73028273	C	T	29	GENIC	homozygous	110936345
2	73028314	73028315	A	C	35	GENIC	homozygous	109828525
2	73028487	73028488	A	G	19	GENIC	homozygous	110936346
2	73028557	73028558	G	A	13	GENIC	homozygous	110936347
2	73028589	73028590	T	G	11	GENIC	homozygous	110936348
2	73028802	73028803	C	T	27	GENIC	homozygous	110936349
2	73028981	73028982	T	C	33	GENIC	homozygous	109828526
2	73029056	73029057	G	A	17	GENIC	homozygous	110936350
2	73029392	73029393	C	T	11	GENIC	homozygous	109828528
2	73029394	73029395	A	T	11	GENIC	homozygous	109828529
2	73029412	73029413	C	G	15	GENIC	homozygous	109828530
2	73029812	73029813	G	A	21	GENIC	homozygous	110936351
2	73028239	73028240	T	A	25	GENIC	homozygous	120124856
2	73029272	73029273	T	A	12	GENIC	homozygous	120365183