chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	204888145	204888146	A	G	26	GENIC	homozygous	61063579
1	204888490	204888491	G	A	32	GENIC	homozygous	61063580
1	204888582	204888583	C	T	36	GENIC	homozygous	61063581
1	204889328	204889329	A	G	29	GENIC	homozygous	61063582
1	204890865	204890866	T	C	34	GENIC	homozygous	61063583
1	204891040	204891041	C	T	31	GENIC	possibly homozygous	61063584
1	204891659	204891661	TT	--	13	GENIC	homozygous	61063585
1	204892234	204892235	T	TACCCAAGCCTGC	40	GENIC	homozygous	61063587
1	204892403	204892404	G	A	39	GENIC	homozygous	61063590
1	204892945	204892946	C	CT	18	GENIC	homozygous	61063591
1	204894369	204894370	C	T	26	GENIC	homozygous	61063593
1	204896004	204896005	G	T	29	GENIC	possibly homozygous	61063594
1	204896187	204896188	C	T	31	GENIC	homozygous	61063595
1	204898480	204898481	A	C	24	GENIC	homozygous	62694696
1	204898507	204898508	T	A	27	GENIC	homozygous	61063596
1	204898742	204898743	G	A	11	GENIC	homozygous	61063597