chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4583372	4583373	T	A	14	GENIC	homozygous	51030564
12	4583626	4583627	G	A	16	GENIC	possibly homozygous	50639771
12	4583727	4583728	G	C	12	GENIC	homozygous	51030567
12	4583755	4583756	C	CA	9	GENIC	homozygous	51030570
12	4583875	4583876	A	G	23	GENIC	homozygous	50394814
12	4584119	4584120	A	G	26	GENIC	homozygous	50394816
12	4584416	4584428	GTGTGTGTGAGT	------------	6	GENIC	heterozygous	50394818
12	4585957	4585958	A	AT	4	GENIC	homozygous	51030573
12	4586561	4586562	A	AGGACAGCCG	1	GENIC	homozygous	50394830
12	4586599	4586600	C	G	19	GENIC	homozygous	51030575
12	4587202	4587203	A	G	18	GENIC	possibly homozygous	50394832
12	4587560	4587561	T	-	2	GENIC	homozygous	50394834
12	4587737	4587738	A	G	12	GENIC	homozygous	51030578
12	4588321	4588322	C	G	11	GENIC	possibly homozygous	51030581
12	4588919	4588920	A	C	10	GENIC	homozygous	50394840
12	4588928	4588929	C	G	14	GENIC	homozygous	50394842
12	4589081	4589082	A	C	19	GENIC	homozygous	50004423
12	4589194	4589195	A	G	1	GENIC	homozygous	50394846
12	4589195	4589196	T	TTTG	1	GENIC	homozygous	51030584
12	4589331	4589332	T	A	14	GENIC	homozygous	50394848
12	4589428	4589429	T	A	13	GENIC	homozygous	50394850
12	4589627	4589628	C	T	8	GENIC	homozygous	50004425
12	4590084	4590085	C	T	4	GENIC	homozygous	50394852
12	4590354	4590355	G	A	22	GENIC	possibly homozygous	51030587
12	4590480	4590481	T	C	17	GENIC	heterozygous	50394854
12	4590798	4590799	A	-	10	GENIC	possibly homozygous	50004427
12	4591044	4591045	G	GA	1	GENIC	homozygous	50394856
12	4591348	4591349	T	A	24	GENIC	possibly homozygous	50394858
12	4591553	4591554	A	C	10	GENIC	homozygous	50394860
12	4591836	4591837	A	G	17	GENIC	homozygous	50394862
12	4584543	4584565	TGTGTGTGTGTGTGTGTGTGTG	----------------------	1	GENIC	homozygous	50732758
12	4585240	4585241	A	-	6	GENIC	homozygous	50842148