chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	226901504	226901505	C	T	29	GENIC	homozygous	108998474
1	226901576	226901577	A	G	41	GENIC	homozygous	108998475
1	226901578	226901579	A	G	40	GENIC	homozygous	108998476
1	226902153	226902154	G	A	27	GENIC	homozygous	108998478
1	226902763	226902764	A	G	32	GENIC	homozygous	108998479
1	226903978	226903979	G	A	26	GENIC	homozygous	108998481
1	226904816	226904817	T	C	14	GENIC	homozygous	108998482
1	226905207	226905208	T	C	32	GENIC	homozygous	108998483
1	226905239	226905240	A	T	35	GENIC	possibly homozygous	108998484
1	226905620	226905621	C	T	16	GENIC	homozygous	108998485
1	226905666	226905667	T	G	25	GENIC	homozygous	108998486
1	226906302	226906303	G	C	26	GENIC	homozygous	108998487
1	226906577	226906578	T	C	22	GENIC	possibly homozygous	108998488
1	226906872	226906873	C	A	22	GENIC	homozygous	108998489
1	226907193	226907194	G	A	14	GENIC	homozygous	108998490
1	226907259	226907260	G	T	18	GENIC	possibly homozygous	108998491
1	226908443	226908444	C	T	31	GENIC	homozygous	108998492
1	226908593	226908594	C	T	28	GENIC	homozygous	108998493
1	226908748	226908749	T	C	25	GENIC	homozygous	108998494
1	226909496	226909497	A	G	28	GENIC	homozygous	108998495
1	226909547	226909548	T	C	34	GENIC	homozygous	108998496
1	226909815	226909816	C	T	29	GENIC	homozygous	108998497
1	226910809	226910810	A	G	33	GENIC	homozygous	108998498
1	226911751	226911752	T	C	26	GENIC	homozygous	108998499
1	226911807	226911808	C	G	20	GENIC	homozygous	108998500
1	226912037	226912038	C	T	19	GENIC	homozygous	108998501