chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	168549218	168549219	A	G	19	GENIC	homozygous	60936121
1	168549613	168549614	T	C	6	GENIC	heterozygous	60936122
1	168550320	168550321	G	GT	11	GENIC	homozygous	60936125
1	168550414	168550415	A	G	16	GENIC	homozygous	60936126
1	168550970	168550971	G	C	19	GENIC	homozygous	60936127
1	168551054	168551055	A	G	15	GENIC	possibly homozygous	60936128
1	168551330	168551331	T	C	15	GENIC	homozygous	60936134
1	168551788	168551789	T	C	12	GENIC	homozygous	60936135
1	168551822	168551823	T	C	18	GENIC	possibly homozygous	60936136
1	168552120	168552121	A	G	10	GENIC	heterozygous	60936137
1	168552358	168552359	T	C	19	GENIC	possibly homozygous	60936138
1	168552424	168552425	A	G	13	GENIC	homozygous	60936139
1	168552573	168552574	A	G	5	GENIC	heterozygous	60936140
1	168553622	168553623	G	A	8	GENIC	possibly homozygous	60936143
1	168553751	168553752	A	G	17	GENIC	homozygous	60936144
1	168553924	168553925	C	T	9	GENIC	homozygous	60936145
1	168553934	168553935	C	T	7	GENIC	homozygous	60936146
1	168554101	168554102	A	AT	4	GENIC	homozygous	60936147
1	168554397	168554398	A	AT	11	GENIC	heterozygous	60936148
1	168554833	168554834	T	TGTGA	7	GENIC	heterozygous	60936149
1	168555250	168555251	C	CAAAG	5	GENIC	homozygous	60936150
1	168555460	168555461	G	A	14	GENIC	homozygous	61552831
1	168555557	168555558	G	A	11	GENIC	homozygous	60936153
1	168555650	168555651	T	C	11	GENIC	heterozygous	60936154
1	168555688	168555689	A	-	10	GENIC	possibly homozygous	60936155
1	168555766	168555767	G	A	12	GENIC	homozygous	60936156
1	168556125	168556126	T	C	18	GENIC	homozygous	61552832
1	168556489	168556490	T	G	12	GENIC	homozygous	61552833
1	168556567	168556568	A	G	15	GENIC	possibly homozygous	61552834
1	168556852	168556853	G	C	11	GENIC	homozygous	60936166