chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	105016886	105016887	A	C	16	GENIC	homozygous	109961998
2	105019640	105019641	A	G	15	GENIC	homozygous	109962000
2	105020239	105020240	C	T	27	GENIC	homozygous	109962002
2	105020353	105020354	G	A	27	GENIC	homozygous	109962004
2	105020921	105020922	G	A	11	GENIC	homozygous	109962006
2	105021105	105021106	C	T	7	GENIC	homozygous	109962008
2	105021146	105021147	C	G	5	GENIC	homozygous	109962010
2	105022220	105022221	C	A	4	GENIC	heterozygous	121444922
2	105019069	105019070	T		15	GENIC	homozygous	127660618
2	105021295	105021296	C	T	17	GENIC	heterozygous	110724608
2	105021326	105021327	G	A	12	GENIC	heterozygous	127799822
2	105023043	105023044	C	T	11	GENIC	heterozygous	127799824
2	105023244	105023245	A	G	5	GENIC	heterozygous	110580312
2	105023625	105023626	G	C	4	GENIC	heterozygous	130263817
2	105024915	105024916	A	G	6	GENIC	heterozygous	127799829
2	105025550	105025551	A	C	9	GENIC	heterozygous	127799831
2	105025607	105025608	T	C	4	GENIC	heterozygous	111328575
2	105025733	105025734	C	A	7	GENIC	homozygous	109962014
2	105025898	105025899	C	T	12	GENIC	heterozygous	109962018
2	105026096	105026096		A	4	GENIC	heterozygous	127660619
2	105026100	105026101	T	C	4	GENIC	heterozygous	127799833
2	105026524	105026525	C	G	3	GENIC	homozygous	127799834
2	105026657	105026658	T	C	13	GENIC	heterozygous	127799835
2	105026855	105026856	G	A	9	GENIC	homozygous	110724614
2	105026989	105026991	AT		21	GENIC	homozygous	127660620
2	105027043	105027044	A	G	20	GENIC	homozygous	109962019
2	105027251	105027252	G	T	16	GENIC	homozygous	109962021
2	105027389	105027390	C	G	13	GENIC	homozygous	109962023
2	105027410	105027414	AGAT		13	GENIC	homozygous	127660621
2	105027563	105027564	A	C	14	GENIC	homozygous	109962025
2	105029318	105029319	C	A	10	GENIC	homozygous	109962027
2	105029712	105029713	T	C	17	GENIC	homozygous	109962029
2	105044760	105044761	A	T	10	GENIC	homozygous	109962031
2	105045764	105045765	T	G	16	GENIC	homozygous	109962033