chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51791834	51791835	T	C	22	GENIC	homozygous	114344026
13	51792188	51792189	G	C	32	GENIC	homozygous	115182407
13	51792260	51792261	G	C	26	GENIC	homozygous	114763572
13	51792265	51792266	T	C	25	GENIC	homozygous	114763574
13	51793598	51793599	A	C	24	GENIC	homozygous	114344030
13	51794293	51794294	G	A	22	GENIC	possibly homozygous	114763576
13	51794355	51794356	A	G	21	GENIC	homozygous	114763578
13	51794560	51794561	T	A	10	GENIC	homozygous	115067257
13	51794578	51794579	G	A	9	GENIC	homozygous	115067259
13	51794862	51794863	A	G	13	GENIC	possibly homozygous	114763580
13	51795344	51795345	A	T	36	GENIC	possibly homozygous	114763582
13	51795787	51795788	C	T	32	GENIC	possibly homozygous	114763584
13	51796060	51796061	G	A	28	GENIC	homozygous	114763586
13	51797123	51797124	G	T	33	GENIC	possibly homozygous	114763588
13	51798128	51798129	T	C	22	GENIC	possibly homozygous	114763590
13	51798210	51798211	C	G	32	GENIC	possibly homozygous	114763592
13	51800190	51800191	A	G	25	GENIC	possibly homozygous	114763594