chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	204836556	204836557	A	G	26	GENIC	homozygous	61063451
1	204836728	204836729	G	A	1	GENIC	homozygous	61063452
1	204836857	204836858	G	GCAGCC	1	GENIC	homozygous	61063455
1	204837027	204837028	A	G	8	GENIC	homozygous	61063456
1	204837242	204837243	G	A	17	GENIC	possibly homozygous	61063457
1	204837636	204837637	A	G	7	GENIC	heterozygous	61063458
1	204838122	204838123	T	C	17	GENIC	homozygous	61063459
1	204838358	204838359	G	T	19	GENIC	homozygous	61063460
1	204838669	204838670	G	C	19	GENIC	homozygous	61063461
1	204838856	204838857	C	T	27	GENIC	possibly homozygous	61063462
1	204842541	204842542	G	A	16	GENIC	possibly homozygous	61063464
1	204842608	204842609	A	AAG	12	GENIC	possibly homozygous	61063465
1	204842790	204842791	A	T	4	GENIC	heterozygous	62095796
1	204843365	204843366	G	A	21	GENIC	possibly homozygous	61063468
1	204843983	204843984	C	G	17	GENIC	heterozygous	61063469
1	204844200	204844201	A	G	8	GENIC	possibly homozygous	61063470
1	204844208	204844209	A	C	9	GENIC	possibly homozygous	61063471
1	204844924	204844925	G	T	2	GENIC	heterozygous	61063488
1	204845485	204845486	A	G	10	GENIC	possibly homozygous	61063489
1	204847110	204847111	G	A	26	GENIC	homozygous	61063490
1	204847392	204847393	G	A	27	GENIC	possibly homozygous	61063491
1	204847730	204847731	G	-	24	GENIC	homozygous	61063492
1	204849531	204849532	T	C	10	GENIC	homozygous	61063493
1	204850607	204850608	A	C	24	GENIC	homozygous	61063496
1	204850875	204850876	C	T	3	GENIC	heterozygous	61063497
1	204851126	204851127	C	CT	3	GENIC	homozygous	61063503
1	204851455	204851456	C	G	14	GENIC	heterozygous	61063504
1	204851491	204851492	T	C	14	GENIC	possibly homozygous	61063505
1	204852919	204852920	G	A	23	GENIC	homozygous	61063506
1	204853056	204853057	C	T	14	GENIC	homozygous	61063507
1	204853279	204853280	G	A	23	GENIC	homozygous	61063508
1	204854131	204854132	G	GC	6	GENIC	homozygous	61063509