chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45293185	45293186	G	A	38	GENIC	homozygous	51873286
10	45293761	45293762	A	G	27	GENIC	homozygous	51873289
10	45294586	45294587	G	C	23	GENIC	homozygous	51873292
10	45295532	45295533	C	T	28	GENIC	homozygous	51873295
10	45296322	45296323	C	A	17	GENIC	homozygous	51873298
10	45296404	45296405	C	CTTTTTT	9	GENIC	possibly homozygous	51442173
10	45296404	45296405	C	CTTTTT	9	GENIC	heterozygous	51873301
10	45296422	45296423	C	T	17	GENIC	heterozygous	51636184
10	45297863	45297864	T	C	22	GENIC	homozygous	51442174
10	45297896	45297897	T	C	23	GENIC	homozygous	51873304
10	45298059	45298060	C	-	19	GENIC	homozygous	51442175
10	45301315	45301316	G	GAA	5	GENIC	heterozygous	51442183
10	45301315	45301316	G	GAAA	5	GENIC	heterozygous	51442184
10	45301703	45301704	G	-	14	GENIC	homozygous	51873307
10	45301706	45301715	GGAAAAAAA	---------	14	GENIC	homozygous	51873310
10	45301842	45301843	T	A	23	GENIC	homozygous	51873313
10	45301961	45301962	A	-	18	GENIC	homozygous	51873316
10	45302562	45302563	T	C	30	GENIC	homozygous	51873319
10	45302987	45302988	T	G	24	GENIC	homozygous	51873322
10	45303308	45303309	T	C	31	GENIC	homozygous	51442189
10	45303587	45303588	T	G	16	GENIC	homozygous	51442190
10	45304860	45304861	C	CAAAA	2	GENIC	homozygous	51442191
10	45305035	45305036	A	ATG	11	GENIC	heterozygous	51442192
10	45305066	45305067	T	TGC	17	GENIC	heterozygous	51873325
10	45305099	45305103	TATA	----	18	GENIC	possibly homozygous	51873328
10	45307032	45307034	AA	--	13	GENIC	homozygous	51636192
10	45307077	45307078	C	CT	14	GENIC	homozygous	51873331
10	45307643	45307644	C	T	14	GENIC	homozygous	51873334
10	45308017	45308020	AGG	---	26	GENIC	homozygous	51873336
10	45305066	45305067	T	C	23	GENIC	heterozygous	51985880