chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94207676	94207677	A	T	14	GENIC	homozygous	51548260
10	94207678	94207679	G	T	14	GENIC	homozygous	51548261
10	94207970	94207971	T	G	14	GENIC	homozygous	51548262
10	94208061	94208065	CCCC	----	10	GENIC	homozygous	51548263
10	94208594	94208595	T	C	20	GENIC	homozygous	51548264
10	94209458	94209459	A	C	16	GENIC	homozygous	51548265
10	94209473	94209474	C	T	16	GENIC	homozygous	51548266
10	94209916	94209917	G	A	21	GENIC	homozygous	51548267
10	94209997	94209999	AG	--	30	GENIC	homozygous	51548268
10	94211632	94211633	G	T	13	GENIC	homozygous	51746431
10	94213238	94213239	C	T	13	INTERGENIC	homozygous	51548270
10	94213510	94213511	T	G	8	INTERGENIC	homozygous	51548271
10	94213696	94213697	T	C	9	INTERGENIC	homozygous	51548273
10	94213725	94213726	C	T	7	INTERGENIC	homozygous	52732883
10	94214292	94214293	G	A	8	INTERGENIC	homozygous	51548279
10	94215290	94215302	AATTTTAAAACA	------------	12	INTERGENIC	homozygous	51548280
10	94215870	94215871	G	GC	11	INTERGENIC	homozygous	51548281
10	94215910	94215911	A	G	14	INTERGENIC	homozygous	51548282
10	94220295	94220296	C	T	16	GENIC	homozygous	52510948
10	94221056	94221060	GTTT	----	6	GENIC	homozygous	51746458
10	94221080	94221081	G	A	9	GENIC	homozygous	52510950
10	94222843	94222844	A	G	16	GENIC	homozygous	51548287
10	94223986	94223987	C	T	16	GENIC	homozygous	52510952
10	94223982	94223983	A	G	15	GENIC	homozygous	51548290
10	94224335	94224336	C	A	14	GENIC	homozygous	52510954
10	94225169	94225171	AC	--	15	GENIC	homozygous	51548294
10	94227689	94227690	C	T	27	GENIC	homozygous	52510956