chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	52562980	52562981	C	T	22	GENIC	homozygous	115356626
12	52563287	52563288	A	G	18	GENIC	homozygous	115356627
12	52564237	52564238	T	C	13	GENIC	homozygous	115356628
12	52564584	52564585	C	T	32	GENIC	homozygous	115356630
12	52565118	52565119	G	A	24	GENIC	possibly homozygous	115356631
12	52566435	52566436	A	G	26	GENIC	homozygous	115356632
12	52568272	52568273	A	G	26	GENIC	homozygous	115356634
12	52568677	52568678	G	T	23	GENIC	homozygous	115356635
12	52569100	52569101	T	A	19	GENIC	homozygous	115356636
12	52570576	52570577	G	A	28	GENIC	homozygous	115356637
12	52571042	52571043	T	A	20	GENIC	homozygous	115356638
12	52571368	52571369	T	C	18	GENIC	homozygous	115356639
12	52571613	52571614	A	G	29	GENIC	homozygous	115356640
12	52571858	52571859	A	T	22	GENIC	homozygous	115404591
12	52572784	52572785	T	G	15	GENIC	homozygous	115404593
12	52572787	52572788	A	C	15	GENIC	homozygous	115404595
12	52573929	52573930	G	C	15	GENIC	homozygous	115356641
12	52574181	52574182	G	A	5	GENIC	homozygous	115516269
12	52575060	52575061	T	C	21	GENIC	homozygous	115356643
12	52575644	52575645	A	G	11	GENIC	homozygous	115356644
12	52576060	52576061	T	G	23	GENIC	homozygous	115356645
12	52576542	52576543	T	C	24	GENIC	homozygous	115404597
12	52576770	52576771	C	A	18	GENIC	homozygous	115356646
12	52577111	52577112	A	G	23	GENIC	homozygous	115356647
12	52577874	52577875	A	G	36	GENIC	homozygous	115356649
12	52578856	52578857	C	T	28	GENIC	homozygous	115404599
12	52579711	52579712	G	C	26	GENIC	homozygous	115356650
12	52584342	52584343	C	T	20	GENIC	homozygous	115356652
12	52587413	52587414	A	C	25	GENIC	homozygous	115356653
12	52594242	52594243	T	G	23	GENIC	homozygous	115356655
12	52595237	52595238	A	G	22	GENIC	homozygous	115356656