chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94192072	94192073	A	G	50	GENIC	homozygous	51548236
10	94192918	94192919	A	C	20	GENIC	homozygous	51548237
10	94193192	94193193	G	A	38	GENIC	homozygous	51548238
10	94193826	94193827	G	A	29	GENIC	possibly homozygous	51548239
10	94194397	94194398	A	G	44	GENIC	homozygous	51548240
10	94194630	94194631	A	G	25	GENIC	homozygous	51548241
10	94194648	94194649	G	A	28	GENIC	homozygous	51548242
10	94195266	94195267	A	-	31	GENIC	homozygous	51548243
10	94195599	94195601	AA	--	19	GENIC	homozygous	51548244
10	94196192	94196193	G	C	17	GENIC	homozygous	51548245
10	94196297	94196298	T	C	27	GENIC	homozygous	51548246
10	94197185	94197186	G	A	35	GENIC	homozygous	51548247
10	94198408	94198409	G	T	46	GENIC	homozygous	51548248
10	94198487	94198488	T	C	35	GENIC	homozygous	51548249
10	94198514	94198515	C	T	29	GENIC	homozygous	51548250
10	94198525	94198526	C	A	29	GENIC	homozygous	51548251
10	94198692	94198693	A	C	36	GENIC	homozygous	51548252
10	94200889	94200890	C	G	36	GENIC	homozygous	51548253
10	94201292	94201293	G	C	32	GENIC	homozygous	51548254
10	94201950	94201951	A	G	41	GENIC	homozygous	51548255
10	94202084	94202085	A	G	21	GENIC	homozygous	51548256
10	94203861	94203862	T	C	37	GENIC	homozygous	51548257
10	94204870	94204871	A	G	47	GENIC	heterozygous	51548258
10	94192609	94192610	A	C	38	GENIC	homozygous	52167447