chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56010732	56010733	T	C	26	GENIC	homozygous	109737584
19	56011013	56011014	C	T	21	GENIC	homozygous	109737586
19	56011203	56011204	C	T	18	GENIC	homozygous	109737588
19	56011543	56011544	T	C	19	GENIC	homozygous	109789091
19	56011979	56011980	C	T	23	GENIC	homozygous	109737590
19	56012029	56012030	G	A	21	GENIC	homozygous	109737592
19	56012468	56012469	C	A	26	GENIC	homozygous	109737594
19	56012835	56012836	T	C	32	GENIC	homozygous	109737596
19	56014649	56014650	C	G	18	GENIC	homozygous	109737598
19	56014664	56014665	A	G	17	GENIC	homozygous	109737600
19	56014888	56014889	A	T	23	GENIC	homozygous	109737602
19	56015842	56015843	G	A	10	GENIC	homozygous	119633646
19	56016113	56016114	C	A	8	GENIC	homozygous	109737604
19	56016888	56016889	G	A	12	GENIC	homozygous	109737606
19	56017375	56017376	C	T	19	GENIC	homozygous	109737608
19	56017436	56017437	T	A	17	GENIC	homozygous	109737610
19	56017846	56017847	T	A	21	GENIC	homozygous	109825770
19	56017905	56017906	T	C	28	GENIC	homozygous	109737612
19	56018570	56018571	G	A	24	GENIC	homozygous	109737614
19	56019292	56019293	T	C	16	GENIC	homozygous	109737616
19	56019695	56019696	C	T	14	GENIC	homozygous	109737618
19	56019753	56019754	A	G	22	GENIC	homozygous	109737620
19	56019944	56019945	C	T	25	GENIC	homozygous	109737622
19	56020046	56020047	G	T	20	GENIC	homozygous	119633647
19	56020331	56020332	G	A	26	GENIC	homozygous	109737624
19	56020497	56020498	T	C	20	GENIC	homozygous	109737626
19	56021246	56021247	T	C	12	GENIC	heterozygous	119633648
19	56021265	56021266	T	C	8	GENIC	homozygous	119633649