chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	57554806	57554807	T	C	9	GENIC	homozygous	109742048
19	57558528	57558529	A	T	15	GENIC	homozygous	109742050
19	57559502	57559503	T	C	13	GENIC	homozygous	109790953
19	57559679	57559680	A	G	10	GENIC	homozygous	109790955
19	57562130	57562131	C	G	12	GENIC	homozygous	109790957
19	57565103	57565104	T	G	12	GENIC	homozygous	109790959
19	57565357	57565358	A	T	8	GENIC	homozygous	109790961
19	57566645	57566646	C	A	13	GENIC	homozygous	109742060
19	57566871	57566872	G	A	9	GENIC	homozygous	109790963
19	57567064	57567065	T	C	13	GENIC	homozygous	109742062
19	57569041	57569042	T	C	8	GENIC	homozygous	109742064
19	57571557	57571558	A	G	6	GENIC	homozygous	109742066
19	57572580	57572581	G	A	5	GENIC	homozygous	109790965
19	57575734	57575735	T	G	8	GENIC	homozygous	109742076
19	57578614	57578615	A	C	8	GENIC	homozygous	109742080
19	57581527	57581528	C	A	8	GENIC	homozygous	109790967
19	57583481	57583482	G	A	8	GENIC	homozygous	109790969
19	57584730	57584731	C	G	6	GENIC	homozygous	109742102
19	57584734	57584735	T	A	6	GENIC	homozygous	109790971
19	57588032	57588033	C	T	5	GENIC	homozygous	109790973
19	57588715	57588716	A	G	12	GENIC	homozygous	109790975
19	57589500	57589501	C	T	12	GENIC	homozygous	109790977