chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	57554806	57554807	T	C	53	GENIC	homozygous	109742048
19	57557690	57557691	C	T	16	GENIC	homozygous	109987365
19	57557894	57557895	G	A	18	GENIC	homozygous	109987367
19	57557935	57557936	T	C	19	GENIC	homozygous	109987369
19	57558528	57558529	A	T	35	GENIC	homozygous	109742050
19	57559502	57559503	T	C	38	GENIC	homozygous	109790953
19	57559679	57559680	A	G	43	GENIC	homozygous	109790955
19	57565357	57565358	A	T	42	GENIC	homozygous	109790961
19	57566645	57566646	C	A	28	GENIC	homozygous	109742060
19	57566871	57566872	G	A	26	GENIC	homozygous	109790963
19	57567064	57567065	T	C	14	GENIC	homozygous	109742062
19	57569041	57569042	T	C	35	GENIC	homozygous	109742064
19	57571557	57571558	A	G	26	GENIC	homozygous	109742066
19	57571810	57571811	A	G	43	GENIC	homozygous	109742068
19	57572580	57572581	G	A	32	GENIC	homozygous	109790965
19	57575734	57575735	T	G	29	GENIC	homozygous	109742076
19	57576995	57576996	A	G	8	GENIC	homozygous	110050194
19	57578614	57578615	A	C	21	GENIC	homozygous	109742080
19	57581527	57581528	C	A	22	GENIC	homozygous	109790967
19	57583481	57583482	G	A	44	GENIC	homozygous	109790969
19	57588032	57588033	C	T	25	GENIC	homozygous	109790973
19	57588715	57588716	A	G	32	GENIC	homozygous	109790975
19	57589500	57589501	C	T	40	GENIC	homozygous	109790977
19	57565287	57565288	C	A	35	GENIC	homozygous	109998452