chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	134610888	134610889	G	C	14	GENIC	homozygous	137628289
5	134611275	134611276	C	A	22	GENIC	homozygous	137628290
5	134611526	134611527	G	A	15	GENIC	homozygous	137628291
5	134615160	134615161	T	C	18	GENIC	homozygous	137628292
5	134615622	134615623	A	C	17	GENIC	homozygous	137628293
5	134615676	134615677	A	G	12	GENIC	homozygous	137628294
5	134615860	134615861	A		11	GENIC	heterozygous	403159126
5	134615860	134615861	A	C	11	GENIC	heterozygous	403159127
5	134616525	134616526	G	A	13	GENIC	possibly homozygous	137628295
5	134617537	134617538	T		8	GENIC	homozygous	403159128
5	134617537	134617538	T	A	8	GENIC	heterozygous	403159129
5	134617561	134617562	T	A	9	GENIC	homozygous	403159130
5	134617561	134617562	T		9	GENIC	heterozygous	403159131
5	134617563	134617564	T	A	9	GENIC	homozygous	403159132
5	134617563	134617564	T		9	GENIC	heterozygous	403159133
5	134617879	134617880	C	T	16	GENIC	homozygous	137628296
5	134622747	134622748	A	G	15	GENIC	homozygous	137628300
5	134617959	134617960	C	T	14	GENIC	homozygous	137628297
5	134619788	134619789	T	C	10	GENIC	homozygous	137628298
5	134619958	134619959	T	C	20	GENIC	homozygous	137628299