chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106503653	106503654	A	G	19	GENIC	homozygous	51765909
10	106503734	106503735	T	C	21	GENIC	homozygous	51765911
10	106503786	106503787	A	G	17	GENIC	homozygous	51765913
10	106504017	106504018	T	G	22	GENIC	homozygous	51765915
10	106504040	106504041	C	T	18	GENIC	homozygous	51765917
10	106504041	106504042	A	G	18	GENIC	homozygous	51765919
10	106504053	106504054	G	C	19	GENIC	homozygous	51765921
10	106504077	106504078	C	T	14	GENIC	homozygous	51765923
10	106504096	106504097	G	A	14	GENIC	homozygous	51765925
10	106504521	106504522	C	T	19	GENIC	homozygous	51765927
10	106504875	106504876	A	G	19	GENIC	homozygous	51765929
10	106504903	106504904	T	C	23	GENIC	homozygous	51765931
10	106504906	106504907	G	A	26	GENIC	homozygous	51765933
10	106505017	106505018	A	G	29	GENIC	homozygous	51765935
10	106505112	106505113	C	G	19	GENIC	homozygous	51765937
10	106505209	106505210	C	T	8	GENIC	homozygous	51765939
10	106505366	106505375	GCCAGCTCT	---------	6	GENIC	homozygous	51765941
10	106505526	106505527	C	CTT	5	GENIC	heterozygous	51765945
10	106506241	106506242	G	A	13	GENIC	homozygous	51765947
10	106506557	106506559	GA	--	7	GENIC	homozygous	51765949
10	106506561	106506562	T	C	8	GENIC	homozygous	52331506
10	106506570	106506571	C	T	12	GENIC	possibly homozygous	51765951
10	106506610	106506611	G	GACTTCT	11	GENIC	homozygous	51765953
10	106507070	106507071	A	AAT	20	GENIC	homozygous	51765955
10	106508572	106508573	C	T	18	GENIC	homozygous	53176788
10	106508777	106508778	A	G	9	GENIC	homozygous	51765957
10	106508789	106508820	AGGAGGGGTTAGAGGAGGGGCTTTGGGACTG	-------------------------------	4	GENIC	homozygous	52331508
10	106509892	106509893	G	GTGGTCAGCATACATGCATGTGTAGGTACTTATGTGTGTT	12	GENIC	homozygous	52331510
10	106510167	106510168	C	G	24	GENIC	homozygous	51765963
10	106510711	106510712	T	C	14	GENIC	homozygous	51765965
10	106513095	106513096	A	T	15	GENIC	homozygous	51765967