chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	52225814	52225815	G	-	2	GENIC	heterozygous	51645581
10	52228518	52228519	G	T	2	GENIC	homozygous	51454276
10	52228896	52228897	C	CTGTA	3	GENIC	heterozygous	52318598
10	52286145	52286146	G	T	7	GENIC	possibly homozygous	51882217
10	52286560	52286561	C	T	24	GENIC	homozygous	51882220
10	52286790	52286791	T	A	9	GENIC	possibly homozygous	51454344
10	52289263	52289264	T	C	11	GENIC	homozygous	51454346
10	52290854	52290855	C	A	12	GENIC	possibly homozygous	51882223
10	52292913	52292914	A	T	28	GENIC	possibly homozygous	51882226
10	52296566	52296567	A	C	24	GENIC	homozygous	51454380
10	52298219	52298220	T	-	2	GENIC	heterozygous	51454391
10	52298255	52298256	G	A	10	GENIC	homozygous	51882229
10	52299132	52299133	A	G	22	GENIC	homozygous	51882232
10	52299961	52299962	G	-	17	GENIC	possibly homozygous	51645649
10	52300296	52300297	A	T	13	GENIC	homozygous	51645650
10	52300363	52300364	C	T	25	GENIC	possibly homozygous	51645651
10	52300571	52300572	A	G	23	GENIC	homozygous	51645652
10	52301109	52301110	G	GA	12	GENIC	possibly homozygous	51454397
10	52301573	52301574	G	A	29	GENIC	possibly homozygous	51454399