chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	57502359	57502360	T	C	16	GENIC	homozygous	109790823
19	57502839	57502840	C	G	5	GENIC	homozygous	109979281
19	57503082	57503083	C	T	7	GENIC	homozygous	109998388
19	57503598	57503599	C	A	16	GENIC	homozygous	109998390
19	57505787	57505788	T	C	15	GENIC	homozygous	109790835
19	57505807	57505808	C	T	18	GENIC	homozygous	109790837
19	57505830	57505831	C	T	21	GENIC	homozygous	109998392
19	57505848	57505849	G	A	17	GENIC	homozygous	109998394
19	57506124	57506125	T	C	4	GENIC	homozygous	109790839
19	57506319	57506320	C	A	9	GENIC	homozygous	109998396
19	57506472	57506473	A	G	10	GENIC	homozygous	109790841
19	57506567	57506568	G	A	17	GENIC	homozygous	109998398
19	57506585	57506586	T	C	16	GENIC	homozygous	109790843
19	57506903	57506904	C	T	22	GENIC	homozygous	109998400
19	57506780	57506781	T	G	23	GENIC	homozygous	109741862
19	57507350	57507351	T	C	22	GENIC	homozygous	109790847
19	57509550	57509551	A	G	15	GENIC	homozygous	109998404
19	57510781	57510782	C	A	18	GENIC	homozygous	109790854
19	57511022	57511023	A	G	10	GENIC	homozygous	109741868
19	57512931	57512932	T	C	27	GENIC	homozygous	109998407
19	57513142	57513143	A	G	15	GENIC	homozygous	109790856
19	57513592	57513593	A	G	18	GENIC	homozygous	109998409
19	57513882	57513883	G	A	22	GENIC	homozygous	109790858
19	57513991	57513992	A	T	18	GENIC	homozygous	109741878
19	57514509	57514510	A	G	2	GENIC	homozygous	109741880