chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4583875	4583876	A	G	21	GENIC	homozygous	50394814
12	4584119	4584120	A	G	21	GENIC	homozygous	50394816
12	4584416	4584428	GTGTGTGTGAGT	------------	3	GENIC	homozygous	50394818
12	4584453	4584454	C	T	12	GENIC	possibly homozygous	50394824
12	4585019	4585020	G	A	17	GENIC	possibly homozygous	50394826
12	4585237	4585238	T	C	15	GENIC	possibly homozygous	50394828
12	4586561	4586562	A	AGGACAGCCG	5	GENIC	heterozygous	50394830
12	4587202	4587203	A	G	24	GENIC	homozygous	50394832
12	4587560	4587561	T	-	1	GENIC	homozygous	50394834
12	4588919	4588920	A	C	7	GENIC	homozygous	50394840
12	4588928	4588929	C	G	10	GENIC	homozygous	50394842
12	4589081	4589082	A	C	20	GENIC	homozygous	50004423
12	4589191	4589192	T	TTTG	2	GENIC	homozygous	50394844
12	4589194	4589195	A	T	2	GENIC	homozygous	50503207
12	4589331	4589332	T	A	10	GENIC	heterozygous	50394848
12	4589428	4589429	T	A	17	GENIC	homozygous	50394850
12	4589627	4589628	C	T	7	GENIC	possibly homozygous	50004425
12	4590084	4590085	C	T	8	GENIC	homozygous	50394852
12	4590480	4590481	T	C	22	GENIC	homozygous	50394854
12	4590798	4590799	A	-	4	GENIC	homozygous	50004427
12	4591044	4591045	G	GA	3	GENIC	homozygous	50394856
12	4591348	4591349	T	A	12	GENIC	homozygous	50394858
12	4591553	4591554	A	C	30	GENIC	possibly homozygous	50394860
12	4591836	4591837	A	G	23	GENIC	possibly homozygous	50394862
12	4592047	4592048	C	T	19	GENIC	homozygous	50394864