chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	104477431	104477432	G	T	30	GENIC	homozygous	971585614
1	104477450	104477451	G	A	33	GENIC	homozygous	971585615
1	104477451	104477452	A	C	31	GENIC	homozygous	971585616
1	104478219	104478220	C	T	28	GENIC	homozygous	971585617
1	104478304	104478305	C	T	32	GENIC	homozygous	971585618
1	104478470	104478471	G	A	30	GENIC	homozygous	971585619
1	104478570	104478571	G	A	23	GENIC	possibly homozygous	971585620
1	104478785	104478786	A	G	22	GENIC	homozygous	971585621
1	104478921	104478922	T	C	27	GENIC	homozygous	971585622
1	104479048	104479049	G	C	31	GENIC	possibly homozygous	971585623
1	104479358	104479359	T	C	31	GENIC	homozygous	971585624
1	104479677	104479678	C	T	34	GENIC	homozygous	971585625
1	104480400	104480401	G	A	21	GENIC	homozygous	971585626
1	104480826	104480827	A	C	18	GENIC	possibly homozygous	971585627
1	104480929	104480930	A	G	27	GENIC	homozygous	971585628
1	104481234	104481235	A	G	20	GENIC	homozygous	971585629