chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	204836556	204836557	A	G	18	GENIC	homozygous	61063451
1	204836857	204836858	G	GCAGCC	6	GENIC	homozygous	61063455
1	204837027	204837028	A	G	15	GENIC	homozygous	61063456
1	204837237	204837238	C	T	13	GENIC	possibly homozygous	62301558
1	204837636	204837637	A	G	14	GENIC	homozygous	61063458
1	204838122	204838123	T	C	31	GENIC	possibly homozygous	61063459
1	204839081	204839082	C	T	22	GENIC	possibly homozygous	62301559
1	204842608	204842609	A	AAG	8	GENIC	homozygous	61063465
1	204843983	204843984	C	G	12	GENIC	heterozygous	61063469
1	204844024	204844025	C	T	20	GENIC	homozygous	62301560
1	204844200	204844201	A	G	13	GENIC	homozygous	61063470
1	204844208	204844209	A	C	14	GENIC	homozygous	61063471
1	204844924	204844925	G	T	1	GENIC	homozygous	61063488
1	204845485	204845486	A	G	4	GENIC	homozygous	61063489
1	204846330	204846331	C	A	14	GENIC	homozygous	62301561
1	204847489	204847490	C	T	28	GENIC	possibly homozygous	62301562
1	204847692	204847693	G	T	31	GENIC	possibly homozygous	62301563
1	204847730	204847731	G	-	16	GENIC	homozygous	61063492
1	204848540	204848541	G	A	11	GENIC	possibly homozygous	62301564
1	204849531	204849532	T	C	11	GENIC	possibly homozygous	61063493
1	204849542	204849543	G	A	10	GENIC	homozygous	62301565
1	204850875	204850876	C	T	6	GENIC	homozygous	61063497
1	204851011	204851012	A	G	2	GENIC	heterozygous	61063501
1	204851124	204851125	T	TC	4	GENIC	homozygous	62301566
1	204851491	204851492	T	C	12	GENIC	homozygous	61063505
1	204851646	204851647	G	A	27	GENIC	homozygous	62301567
1	204852398	204852399	T	G	21	GENIC	homozygous	62301568
1	204852889	204852890	C	T	23	GENIC	homozygous	62301569
1	204853279	204853280	G	A	25	GENIC	homozygous	61063508
1	204854131	204854132	G	GC	6	GENIC	homozygous	61063509