chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	54573720	54573721	G	A	20	GENIC	homozygous	114674504
13	54573740	54573741	A	G	16	GENIC	homozygous	114552063
13	54573744	54573745	C	T	16	GENIC	homozygous	114552064
13	54573765	54573766	T	A	11	GENIC	homozygous	114674506
13	54573966	54573967	C	T	27	GENIC	homozygous	114674508
13	54574510	54574511	T	C	24	GENIC	homozygous	114552069
13	54574761	54574762	G	C	31	GENIC	homozygous	114552071
13	54575360	54575361	G	A	14	GENIC	homozygous	114552075
13	54575507	54575508	G	A	15	GENIC	homozygous	114674510
13	54576396	54576397	T	C	28	GENIC	homozygous	114552081
13	54576655	54576656	A	G	35	GENIC	homozygous	114552083
13	54576692	54576693	C	T	42	GENIC	homozygous	114552084
13	54576937	54576938	A	T	21	GENIC	homozygous	114552085
13	54577884	54577885	C	T	25	GENIC	homozygous	114674512
13	54578177	54578178	T	C	22	GENIC	homozygous	114552086
13	54579101	54579102	A	G	18	GENIC	homozygous	114674514
13	54579106	54579107	T	C	19	GENIC	homozygous	114674516
13	54579167	54579168	G	A	31	GENIC	homozygous	114674518
13	54579563	54579564	A	G	26	GENIC	homozygous	114552089
13	54579593	54579594	T	C	27	GENIC	homozygous	114674520
13	54579755	54579756	A	G	25	GENIC	homozygous	114674522