chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94262555	94262556	T		33	GENIC	homozygous	128847350
10	94266257	94266258	G	A	35	GENIC	heterozygous	118009241
10	94266305	94266306	C	G	30	GENIC	heterozygous	118051058
10	94266313	94266313		CG	27	GENIC	heterozygous	128847352
10	94266315	94266317	GA		25	GENIC	heterozygous	128847353
10	94266768	94266769	C	T	3	GENIC	homozygous	117228238
10	94266769	94266770	T	C	2	GENIC	homozygous	117228240
10	94266930	94266931	T		40	GENIC	homozygous	128847354
10	94266946	94266946		A	47	GENIC	homozygous	128847355
10	94266986	94266986		A	47	GENIC	homozygous	128847356
10	94266990	94266990		A	48	GENIC	homozygous	128847357
10	94266991	94266991		C	49	GENIC	homozygous	128847358
10	94267025	94267026	T		53	GENIC	homozygous	128847359
10	94267033	94267034	T		54	GENIC	homozygous	128847360
10	94267036	94267037	T		53	GENIC	homozygous	128847361
10	94267259	94267260	A	C	48	GENIC	homozygous	116684998
10	94267259	94267259		C	48	GENIC	homozygous	128847362
10	94267264	94267265	G		49	GENIC	homozygous	128847363