chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	33734701	33734702	T	C	15	GENIC	homozygous	140447474
19	33734835	33734836	C	T	19	GENIC	homozygous	140447475
19	33734973	33734974	G	A	28	GENIC	homozygous	140447476
19	33735445	33735446	T	C	15	GENIC	homozygous	140447477
19	33736333	33736334	C	T	11	GENIC	homozygous	140447478
19	33736404	33736405	C	A	14	GENIC	homozygous	140447479
19	33736417	33736417		A	16	GENIC	possibly homozygous	140387247
19	33736715	33736716	G	T	14	GENIC	homozygous	140447480
19	33736716	33736717	C	G	13	GENIC	homozygous	140447481
19	33736782	33736783	T	C	11	GENIC	homozygous	140447482
19	33736840	33736841	C	T	9	GENIC	homozygous	140447483
19	33737209	33737210	C	T	19	GENIC	homozygous	140447484
19	33737928	33737929	C	T	18	GENIC	homozygous	140447485
19	33737980	33737981	T	C	17	GENIC	homozygous	140447486
19	33737995	33737996	C	G	21	GENIC	homozygous	140447487
19	33740102	33740103	A	T	12	GENIC	homozygous	140447488