chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	65838922	65838923	A	G	17	GENIC	homozygous	51478423
10	65840039	65840040	T	C	24	GENIC	homozygous	51478425
10	65840322	65840326	TTCT	----	14	GENIC	possibly homozygous	52382385
10	65840674	65840675	T	C	10	GENIC	homozygous	51478427
10	65841148	65841149	C	CTT	2	GENIC	heterozygous	51678621
10	65841542	65841543	T	C	16	GENIC	homozygous	51478430
10	65843657	65843658	A	G	20	GENIC	homozygous	51478431
10	65843829	65843830	A	G	27	GENIC	homozygous	51478432
10	65844744	65844745	G	A	15	GENIC	homozygous	51478434
10	65844774	65844775	A	G	3	GENIC	homozygous	51478435
10	65845114	65845115	T	-	7	GENIC	homozygous	51478439
10	65848639	65848643	GGGT	----	10	GENIC	homozygous	51478444
10	65850039	65850040	A	C	27	GENIC	homozygous	51478454
10	65852367	65852368	A	T	20	GENIC	possibly homozygous	51478464
10	65852458	65852459	G	A	26	GENIC	homozygous	51907235
10	65840756	65840757	G	GATTTATTTATTT	2	GENIC	homozygous	51907225
10	65841639	65841640	G	A	20	GENIC	homozygous	51907227
10	65849952	65849953	C	T	37	GENIC	homozygous	51907229
10	65850479	65850480	G	A	22	GENIC	homozygous	51907231
10	65851758	65851759	C	T	37	GENIC	homozygous	51907233
10	65845810	65845811	C	T	22	GENIC	homozygous	52320320
10	65845811	65845812	T	A	22	GENIC	homozygous	52320322
10	65853065	65853066	T	C	28	GENIC	homozygous	51478467