chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52126039	52126040	G	A	25	GENIC	homozygous	114345465
13	52127275	52127276	C	T	30	GENIC	homozygous	114345467
13	52127277	52127278	G	A	31	GENIC	homozygous	114345469
13	52127603	52127604	T	C	17	GENIC	possibly homozygous	114672475
13	52128147	52128148	G	A	15	GENIC	homozygous	114345471
13	52128827	52128828	C	A	27	GENIC	homozygous	114345473
13	52129299	52129300	G	A	30	GENIC	homozygous	114345475
13	52129311	52129312	G	A	29	GENIC	homozygous	114345477
13	52130147	52130148	A	C	26	GENIC	possibly homozygous	114672477
13	52131567	52131568	G	T	37	GENIC	homozygous	115152185
13	52131681	52131682	C	T	37	GENIC	homozygous	114672478
13	52131792	52131793	T	C	20	GENIC	homozygous	114345479
13	52131981	52131982	G	A	17	GENIC	homozygous	114345481
13	52132650	52132651	A	C	14	GENIC	homozygous	114345483
13	52132994	52132995	C	T	29	GENIC	homozygous	114345485
13	52134365	52134366	C	T	28	GENIC	homozygous	114345487
13	52135947	52135948	T	C	33	GENIC	homozygous	114345489
13	52129415	52129416	G	A	26	GENIC	homozygous	114720455
13	52131633	52131634	G	A	28	GENIC	homozygous	118450961
13	52132740	52132741	A	G	18	GENIC	homozygous	114857687