chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	218190162	218190163	G	T	4	GENIC	homozygous	59936859
2	218190485	218190486	C	A	10	GENIC	homozygous	59936860
2	218191389	218191390	G	A	12	GENIC	heterozygous	59936861
2	218191425	218191426	T	G	9	GENIC	homozygous	59397151
2	218191573	218191574	C	T	9	GENIC	homozygous	59936862
2	218193681	218193682	A	C	8	GENIC	homozygous	59936864
2	218193725	218193726	C	CA	1	GENIC	homozygous	60561688
2	218193817	218193818	T	A	12	GENIC	homozygous	59936865
2	218194383	218194384	A	T	17	GENIC	possibly homozygous	59936866
2	218195687	218195688	T	A	14	GENIC	possibly homozygous	59397156
2	218195718	218195719	T	G	18	GENIC	possibly homozygous	59936867
2	218196408	218196409	G	A	3	GENIC	homozygous	59936869
2	218197175	218197176	T	C	7	GENIC	possibly homozygous	59397163
2	218197267	218197268	C	A	5	GENIC	homozygous	59936870
2	218197444	218197445	G	A	7	GENIC	homozygous	59936871
2	218198574	218198575	C	T	12	GENIC	possibly homozygous	59936873
2	218198594	218198595	C	CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	3	GENIC	heterozygous	60457567
2	218199346	218199347	A	T	21	GENIC	possibly homozygous	59936874
2	218201310	218201311	A	-	1	GENIC	homozygous	59397170
2	218202446	218202447	A	G	14	GENIC	homozygous	59397173
2	218204260	218204261	G	A	13	GENIC	heterozygous	59397177
2	218205266	218205267	T	C	13	GENIC	homozygous	59397178
2	218206412	218206413	T	G	9	GENIC	homozygous	59397180