chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51229865	51229866	G	A	23	GENIC	possibly homozygous	114342925
13	51229894	51229895	G	C	23	GENIC	homozygous	114342927
13	51230754	51230754		GA	24	GENIC	homozygous	129053089
13	51231752	51231752		ACAT	13	GENIC	homozygous	129053090
13	51232534	51232535	T	C	24	GENIC	homozygous	114342929
13	51232883	51232884	C	T	21	GENIC	homozygous	114342931
13	51233414	51233415	C	G	25	GENIC	homozygous	114342933
13	51233512	51233513	T	A	21	GENIC	homozygous	114342935
13	51234021	51234022	C	A	28	GENIC	homozygous	114342937
13	51234214	51234215	A	C	26	GENIC	homozygous	114342939
13	51232759	51232760	A	G	21	GENIC	homozygous	114672311
13	51234384	51234385	G	C	10	GENIC	homozygous	114672313
13	51234879	51234880	A		22	GENIC	homozygous	129053091
13	51235431	51235432	G	A	26	GENIC	homozygous	114342941
13	51235884	51235885	C	A	28	GENIC	homozygous	114342943
13	51234322	51234323	C	T	10	GENIC	homozygous	114948051
13	51234804	51234805	A	G	7	GENIC	homozygous	118450765