chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91212371	91212385	GTGTGTGTGCGCGC	--------------	11	GENIC	possibly homozygous	52397291
10	91212529	91212530	G	T	36	GENIC	homozygous	51739170
10	91212860	91212861	G	C	15	GENIC	homozygous	51739172
10	91212866	91212867	C	A	16	GENIC	homozygous	51539279
10	91213176	91213177	A	G	24	GENIC	homozygous	51739174
10	91215204	91215205	T	C	25	GENIC	homozygous	51739176
10	91215900	91215914	ACACAAAATCCCAA	--------------	16	GENIC	heterozygous	52397293
10	91216360	91216361	G	A	25	GENIC	homozygous	51539282
10	91216500	91216503	AAA	---	1	GENIC	homozygous	52397295
10	91216712	91216713	C	T	44	GENIC	homozygous	51539283
10	91217937	91217938	C	-	39	GENIC	homozygous	51739178
10	91217964	91217965	C	T	40	GENIC	homozygous	51739180
10	91218114	91218115	G	-	12	INTERGENIC	possibly homozygous	51739182
10	91218185	91218186	C	T	22	INTERGENIC	homozygous	51739184
10	91218966	91218969	TGA	---	30	GENIC	homozygous	51739186
10	91218969	91218970	A	C	29	GENIC	homozygous	52323339
10	91219687	91219688	G	T	38	GENIC	homozygous	51539284
10	91220452	91220453	A	G	40	GENIC	homozygous	51739188
10	91221216	91221240	TTCTTTTTTTTTTTTTTTTTTTGG	------------------------	25	GENIC	homozygous	51739190
10	91221477	91221478	C	G	26	GENIC	homozygous	51539293
10	91222132	91222133	G	A	41	GENIC	homozygous	51539296