chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	104147573	104147574	A	G	18	GENIC	homozygous	108904617
1	104147811	104147812	C	T	26	GENIC	homozygous	108904618
1	104148247	104148248	A	T	24	GENIC	homozygous	108904619
1	104148251	104148252	T	G	22	GENIC	homozygous	108904620
1	104148336	104148337	G	A	26	GENIC	homozygous	108904621
1	104149232	104149233	A	G	18	GENIC	homozygous	108904622
1	104149369	104149370	A	T	32	GENIC	homozygous	108904623
1	104151058	104151059	G	A	33	GENIC	homozygous	108904628
1	104151367	104151368	T	C	31	GENIC	homozygous	108904629
1	104151563	104151564	A	G	38	GENIC	homozygous	108904630
1	104151856	104151857	C	T	42	GENIC	homozygous	108904631
1	104152447	104152448	A	G	25	GENIC	homozygous	108904632
1	104153703	104153704	A	G	22	GENIC	homozygous	108904635
1	104154255	104154256	G	A	25	GENIC	homozygous	108904636
1	104155693	104155694	C	A	24	GENIC	homozygous	108904637
1	104156010	104156011	G	T	22	GENIC	homozygous	108904638
1	104156232	104156233	C	A	24	GENIC	homozygous	108904639
1	104156536	104156537	C	G	20	GENIC	homozygous	108904640
1	104156649	104156650	A	G	22	GENIC	homozygous	108904641
1	104156754	104156755	A	C	21	GENIC	homozygous	108904642
1	104157564	104157565	A	C	29	GENIC	homozygous	108904643
1	104157620	104157621	G	C	29	GENIC	homozygous	108904644
1	104158483	104158484	G	A	26	GENIC	homozygous	108904645
1	104159793	104159794	C	T	31	GENIC	homozygous	108904646
1	104163324	104163325	T	G	26	GENIC	homozygous	108904648
1	104163398	104163399	T	C	33	GENIC	homozygous	108904649
1	104163823	104163824	G	C	32	GENIC	homozygous	108904650
1	104163878	104163879	C	T	28	GENIC	homozygous	108904651
1	104164020	104164021	G	A	34	GENIC	homozygous	108904652
1	104166200	104166201	A	G	24	GENIC	homozygous	108904653
1	104166247	104166248	C	A	21	GENIC	homozygous	108904654