chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	52371429	52371430	G	A	33	GENIC	possibly homozygous	52627463
8	52371707	52371708	A	G	31	GENIC	homozygous	52627465
8	52372004	52372005	A	G	31	GENIC	homozygous	52627467
8	52373497	52373498	A	G	22	GENIC	homozygous	52627469
8	52373890	52373891	C	CT	26	GENIC	homozygous	52627471
8	52374591	52374592	T	TTC	25	GENIC	homozygous	52627473
8	52375598	52375599	G	A	28	GENIC	homozygous	52627475
8	52375765	52375766	G	-	18	GENIC	homozygous	52627477
8	52376021	52376022	G	A	18	GENIC	possibly homozygous	52627479
8	52376265	52376266	T	TA	23	GENIC	possibly homozygous	52627481
8	52376642	52376643	T	C	21	GENIC	homozygous	52627483
8	52377353	52377354	G	GAGCCAGCTACAAAA	24	GENIC	homozygous	52627485
8	52377589	52377590	C	T	30	GENIC	homozygous	52627489
8	52378432	52378433	A	G	35	GENIC	homozygous	52627491