chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51281022	51281023	C	T	25	GENIC	homozygous	114948055
13	51281641	51281642	C	T	24	GENIC	homozygous	114890601
13	51284549	51284550	A	G	16	GENIC	homozygous	114890603
13	51289681	51289682	T	C	12	GENIC	homozygous	114762996
13	51284626	51284627	A	G	22	GENIC	homozygous	114343039
13	51285025	51285026	G	A	38	GENIC	homozygous	114762986
13	51286651	51286652	C	T	38	GENIC	homozygous	114762990
13	51289682	51289683	T	C	12	GENIC	homozygous	114762998
13	51289814	51289815	G	A	16	GENIC	homozygous	114890605
13	51289892	51289893	T	G	24	GENIC	homozygous	114890607
13	51290558	51290559	T	C	38	GENIC	homozygous	114343041
13	51294186	51294187	C	T	37	GENIC	homozygous	114890609
13	51295938	51295939	G	A	13	GENIC	homozygous	114763002
13	51298693	51298694	G	C	26	GENIC	homozygous	114763008
13	51298694	51298695	G	A	26	GENIC	homozygous	114763010
13	51300057	51300058	C	T	8	GENIC	homozygous	114890611
13	51300596	51300597	G	A	34	GENIC	homozygous	114890613
13	51303692	51303693	T	C	24	GENIC	homozygous	114763014
13	51304115	51304116	G	A	9	GENIC	homozygous	114763018