chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	29594660	29594661	T	A	57	GENIC	homozygous	136061164
2	29594795	29594796	C	T	40	GENIC	homozygous	136061165
2	29595698	29595699	G	A	51	GENIC	homozygous	136061167
2	29595986	29595987	T	C	47	GENIC	homozygous	136061168
2	29596791	29596792	C	G	50	GENIC	homozygous	136061169
2	29598208	29598209	T	A	29	GENIC	homozygous	142928653
2	29599363	29599366	ACC		25	GENIC	homozygous	135895848
2	29600694	29600695	A	G	53	GENIC	homozygous	136061174
2	29602656	29602657	A	T	42	GENIC	homozygous	136061176
2	29602709	29602710	A	T	49	GENIC	homozygous	136061177
2	29602929	29602930	T	C	70	GENIC	homozygous	136061178
2	29605140	29605141	T	A	30	GENIC	homozygous	142928654
2	29605200	29605201	G	A	33	GENIC	homozygous	142928655
2	29606756	29606757	G	A	52	GENIC	homozygous	136061180
2	29607023	29607024	T	C	32	GENIC	homozygous	136061181
2	29607085	29607086	C	A	13	GENIC	homozygous	136061182
2	29607739	29607740	A	G	61	GENIC	homozygous	136061184
2	29608245	29608246	A	G	55	GENIC	homozygous	136061185
2	29608369	29608370	G	A	65	GENIC	homozygous	136061186
2	29608758	29608759	G	A	49	GENIC	homozygous	136061187
2	29609030	29609031	C	T	61	GENIC	homozygous	142928656
2	29610994	29610995	G	A	46	GENIC	homozygous	136061189
2	29612226	29612227	C	T	53	GENIC	homozygous	136061190
2	29612435	29612436	C	T	40	GENIC	homozygous	142928657
2	29612571	29612572	T	C	41	GENIC	homozygous	142928658
2	29612801	29612802	C	A	60	GENIC	homozygous	142928659
2	29607105	29607106	G		9	GENIC	heterozygous	402995985
2	29599419	29599419		CT	10	GENIC	homozygous	144575928
2	29608555	29608556	T		49	GENIC	homozygous	135895850
2	29608950	29608950		T	48	GENIC	possibly homozygous	142892799
2	29607105	29607106	G	A	9	GENIC	homozygous	154066983