chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91212383	91212385	GC	--	10	GENIC	heterozygous	51539278
10	91212866	91212867	C	A	18	GENIC	homozygous	51539279
10	91213234	91213235	C	G	32	GENIC	homozygous	52166056
10	91215806	91215807	C	-	18	GENIC	homozygous	51539280
10	91215848	91215858	GTGTGTGTGT	----------	2	GENIC	homozygous	51539281
10	91216360	91216361	G	A	46	GENIC	homozygous	51539282
10	91216712	91216713	C	T	31	GENIC	homozygous	51539283
10	91216982	91216983	G	C	16	GENIC	homozygous	52166057
10	91217757	91217758	A	G	25	GENIC	homozygous	52166058
10	91217937	91217938	C	-	37	GENIC	homozygous	51739178
10	91217964	91217965	C	T	39	GENIC	homozygous	51739180
10	91218114	91218115	G	-	1	INTERGENIC	homozygous	51739182
10	91218146	91218150	TCTT	----	22	INTERGENIC	homozygous	52166059
10	91219687	91219688	G	T	22	GENIC	homozygous	51539284
10	91219758	91219759	A	ATCTGAGGCC	13	GENIC	homozygous	52166060
10	91220289	91220290	G	A	39	GENIC	homozygous	52166061
10	91220452	91220453	A	G	38	GENIC	homozygous	51739188
10	91220714	91220715	T	C	35	GENIC	homozygous	52166062
10	91220753	91220754	A	T	33	GENIC	homozygous	51539287
10	91221084	91221085	G	A	34	GENIC	homozygous	51539288
10	91221218	91221226	CTTTTTTT	--------	11	GENIC	possibly homozygous	51539289
10	91221219	91221223	TTTT	----	10	GENIC	possibly homozygous	51539290
10	91221294	91221295	C	T	16	GENIC	homozygous	52166063
10	91221477	91221478	C	G	25	GENIC	homozygous	51539293
10	91221580	91221581	C	T	33	GENIC	homozygous	51539294
10	91221634	91221635	A	G	42	GENIC	homozygous	51539295
10	91222132	91222133	G	A	28	GENIC	homozygous	51539296