chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56024903	56024904	G	C	43	GENIC	homozygous	109737636
19	56025461	56025462	T	C	32	GENIC	homozygous	109737638
19	56025891	56025892	C	T	26	GENIC	homozygous	109737640
19	56025938	56025939	G	A	25	GENIC	homozygous	109737642
19	56026088	56026089	T	C	13	GENIC	homozygous	109737644
19	56026303	56026304	T	G	32	GENIC	homozygous	109737646
19	56027719	56027720	A	T	23	GENIC	homozygous	109737648
19	56027952	56027953	C	T	35	GENIC	homozygous	109737650
19	56028555	56028556	T	A	24	GENIC	possibly homozygous	109737652
19	56029181	56029182	A	G	49	GENIC	homozygous	109737654
19	56029468	56029469	A	G	43	GENIC	homozygous	109737656
19	56029649	56029650	C	T	41	GENIC	homozygous	109737658
19	56029973	56029974	G	A	87	GENIC	heterozygous	119633651
19	56029984	56029985	A	G	88	GENIC	heterozygous	119633653
19	56030008	56030009	A	G	84	GENIC	possibly homozygous	119633654
19	56030011	56030012	A	G	84	GENIC	heterozygous	119633655
19	56030038	56030039	A	T	78	GENIC	heterozygous	119666435
19	56030044	56030045	A	G	60	GENIC	heterozygous	119633656
19	56030128	56030129	G	A	24	GENIC	possibly homozygous	109737661
19	56032117	56032118	C	A	11	GENIC	possibly homozygous	110028094