chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	73026732	73026733	T	C	15	GENIC	homozygous	109828518
2	73026783	73026784	A	G	16	GENIC	homozygous	109828519
2	73026786	73026787	A	G	16	GENIC	homozygous	110936342
2	73026862	73026863	T	A	17	GENIC	homozygous	110936343
2	73027051	73027052	T	G	4	GENIC	heterozygous	109828521
2	73027982	73027983	T	C	15	GENIC	homozygous	109828522
2	73028015	73028016	T	C	16	GENIC	homozygous	109828523
2	73028068	73028069	T	C	13	GENIC	homozygous	110936344
2	73028272	73028273	C	T	14	GENIC	homozygous	110936345
2	73028314	73028315	A	C	15	GENIC	homozygous	109828525
2	73028487	73028488	A	G	14	GENIC	homozygous	110936346
2	73028557	73028558	G	A	23	GENIC	homozygous	110936347
2	73028589	73028590	T	G	24	GENIC	homozygous	110936348
2	73028802	73028803	C	T	28	GENIC	homozygous	110936349
2	73028981	73028982	T	C	24	GENIC	homozygous	109828526
2	73029056	73029057	G	A	24	GENIC	homozygous	110936350
2	73029392	73029393	C	T	10	GENIC	homozygous	109828528
2	73029394	73029395	A	T	9	GENIC	homozygous	109828529
2	73029412	73029413	C	G	12	GENIC	homozygous	109828530
2	73029812	73029813	G	A	20	GENIC	homozygous	110936351
2	73028239	73028240	T	A	16	GENIC	homozygous	120124856
2	73029796	73029797	C	T	15	GENIC	homozygous	120229026