chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56010315	56010316	G	A	16	GENIC	homozygous	109943419
19	56010732	56010733	T	C	29	GENIC	homozygous	109737584
19	56011013	56011014	C	T	30	GENIC	homozygous	109737586
19	56011543	56011544	T	C	24	GENIC	homozygous	109789091
19	56011979	56011980	C	T	31	GENIC	homozygous	109737590
19	56012029	56012030	G	A	34	GENIC	homozygous	109737592
19	56012186	56012187	A	G	19	GENIC	homozygous	109943421
19	56012468	56012469	C	A	33	GENIC	homozygous	109737594
19	56012835	56012836	T	C	33	GENIC	homozygous	109737596
19	56014068	56014069	G	A	28	GENIC	homozygous	109943424
19	56014649	56014650	C	G	28	GENIC	homozygous	109737598
19	56014664	56014665	A	G	27	GENIC	homozygous	109737600
19	56014888	56014889	A	T	28	GENIC	homozygous	109737602
19	56016479	56016480	G	A	26	GENIC	homozygous	109943427
19	56017436	56017437	T	A	33	GENIC	homozygous	109737610
19	56017905	56017906	T	C	29	GENIC	homozygous	109737612
19	56018570	56018571	G	A	27	GENIC	homozygous	109737614
19	56019057	56019058	T	C	29	GENIC	homozygous	109943429
19	56019292	56019293	T	C	22	GENIC	homozygous	109737616
19	56019695	56019696	C	T	31	GENIC	homozygous	109737618
19	56019753	56019754	A	G	34	GENIC	homozygous	109737620
19	56019944	56019945	C	T	24	GENIC	homozygous	109737622
19	56020331	56020332	G	A	31	GENIC	homozygous	109737624
19	56020807	56020808	G	A	24	GENIC	homozygous	109943431
19	56017846	56017847	T	A	17	GENIC	homozygous	109825770