chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	29594660	29594661	T	A	17	GENIC	homozygous	136061164
2	29594795	29594796	C	T	15	GENIC	homozygous	136061165
2	29595698	29595699	G	A	26	GENIC	homozygous	136061167
2	29595986	29595987	T	C	13	GENIC	homozygous	136061168
2	29596791	29596792	C	G	23	GENIC	homozygous	136061169
2	29598208	29598209	T	A	8	GENIC	possibly homozygous	142928653
2	29600694	29600695	A	G	17	GENIC	homozygous	136061174
2	29602656	29602657	A	T	21	GENIC	homozygous	136061176
2	29602709	29602710	A	T	24	GENIC	homozygous	136061177
2	29602929	29602930	T	C	21	GENIC	homozygous	136061178
2	29605140	29605141	T	A	25	GENIC	homozygous	142928654
2	29605200	29605201	G	A	22	GENIC	homozygous	142928655
2	29606756	29606757	G	A	15	GENIC	homozygous	136061180
2	29607023	29607024	T	C	13	GENIC	homozygous	136061181
2	29607085	29607086	C	A	7	GENIC	homozygous	136061182
2	29607105	29607106	G	A	5	GENIC	homozygous	154066983
2	29607739	29607740	A	G	19	GENIC	homozygous	136061184
2	29608245	29608246	A	G	28	GENIC	homozygous	136061185
2	29608369	29608370	G	A	29	GENIC	homozygous	136061186
2	29608758	29608759	G	A	31	GENIC	homozygous	136061187
2	29609030	29609031	C	T	20	GENIC	homozygous	142928656
2	29610994	29610995	G	A	23	GENIC	homozygous	136061189
2	29612226	29612227	C	T	27	GENIC	homozygous	136061190
2	29612435	29612436	C	T	15	GENIC	homozygous	142928657
2	29612571	29612572	T	C	13	GENIC	homozygous	142928658
2	29612801	29612802	C	A	17	GENIC	homozygous	142928659
2	29607105	29607106	G		5	GENIC	heterozygous	402995985
2	29599363	29599366	ACC		15	GENIC	homozygous	135895848
2	29608555	29608556	T		21	GENIC	homozygous	135895850
2	29608950	29608950		T	27	GENIC	possibly homozygous	142892799