chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91212529	91212530	G	T	18	GENIC	possibly homozygous	51739170
10	91212860	91212861	G	C	7	GENIC	possibly homozygous	51739172
10	91212866	91212867	C	A	7	GENIC	homozygous	51539279
10	91213176	91213177	A	G	10	GENIC	homozygous	51739174
10	91215204	91215205	T	C	17	GENIC	possibly homozygous	51739176
10	91215805	91215806	G	GC	5	GENIC	heterozygous	51929153
10	91216360	91216361	G	A	21	GENIC	possibly homozygous	51539282
10	91216712	91216713	C	T	18	GENIC	possibly homozygous	51539283
10	91217937	91217938	C	-	11	GENIC	homozygous	51739178
10	91217964	91217965	C	T	14	GENIC	possibly homozygous	51739180
10	91218114	91218115	G	-	3	INTERGENIC	heterozygous	51739182
10	91218185	91218186	C	T	26	INTERGENIC	possibly homozygous	51739184
10	91218966	91218969	TGA	---	7	GENIC	heterozygous	51739186
10	91218969	91218970	A	C	6	GENIC	heterozygous	52323339
10	91219687	91219688	G	T	25	GENIC	possibly homozygous	51539284
10	91220452	91220453	A	G	12	GENIC	homozygous	51739188
10	91221216	91221240	TTCTTTTTTTTTTTTTTTTTTTGG	------------------------	1	GENIC	homozygous	51739190
10	91221477	91221478	C	G	20	GENIC	possibly homozygous	51539293
10	91222132	91222133	G	A	22	GENIC	possibly homozygous	51539296