chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	57502359	57502360	T	C	29	GENIC	homozygous	109790823
19	57502839	57502840	C	G	27	GENIC	homozygous	109979281
19	57502921	57502922	C	T	30	GENIC	homozygous	109790825
19	57502987	57502988	G	A	23	GENIC	homozygous	109790827
19	57503614	57503615	C	G	43	GENIC	homozygous	109790829
19	57503832	57503833	C	T	27	GENIC	homozygous	109979283
19	57503896	57503897	T	C	32	GENIC	homozygous	109790831
19	57505787	57505788	T	C	46	GENIC	homozygous	109790835
19	57505807	57505808	C	T	43	GENIC	homozygous	109790837
19	57506124	57506125	T	C	25	GENIC	homozygous	109790839
19	57506585	57506586	T	C	29	GENIC	homozygous	109790843
19	57506780	57506781	T	G	32	GENIC	homozygous	109741862
19	57507350	57507351	T	C	34	GENIC	homozygous	109790847
19	57507739	57507740	G	A	22	GENIC	homozygous	109790850
19	57510781	57510782	C	A	12	GENIC	homozygous	109790854
19	57511022	57511023	A	G	19	GENIC	homozygous	109741868
19	57513142	57513143	A	G	27	GENIC	homozygous	109790856
19	57513882	57513883	G	A	34	GENIC	homozygous	109790858
19	57513991	57513992	A	T	21	GENIC	homozygous	109741878
19	57514206	57514207	C	T	22	GENIC	homozygous	109790860
19	57514509	57514510	A	G	11	GENIC	homozygous	109741880