chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51240523	51240525	GG	--	19	GENIC	homozygous	49755842
13	51240534	51240536	GT	--	23	GENIC	heterozygous	50036791
13	51240535	51240536	T	-	26	GENIC	heterozygous	50192414
13	51241496	51241497	G	A	21	GENIC	heterozygous	50359748
13	51242890	51242894	TGTC	----	26	GENIC	homozygous	50359750
13	51244642	51244643	A	-	18	GENIC	homozygous	50359752
13	51245764	51245765	G	A	25	GENIC	homozygous	50359754
13	51245852	51245853	A	-	16	GENIC	possibly homozygous	50229937
13	51245865	51245867	AA	--	18	GENIC	possibly homozygous	50359756
13	51250508	51250509	A	G	23	GENIC	possibly homozygous	50359757
13	51251429	51251430	T	G	12	GENIC	homozygous	50359759
13	51252134	51252135	T	C	17	GENIC	heterozygous	50359761
13	51254404	51254405	C	T	21	GENIC	homozygous	50359763
13	51254857	51254858	A	C	30	GENIC	homozygous	50359765
13	51254907	51254908	G	A	35	GENIC	homozygous	50359767
13	51255289	51255290	T	C	18	GENIC	homozygous	50359769
13	51255944	51255958	TTGAACTTCTGACC	--------------	9	GENIC	homozygous	50359771
13	51256033	51256034	C	T	13	GENIC	homozygous	50359773
13	51256311	51256312	G	A	30	GENIC	homozygous	50359775
13	51256344	51256345	T	C	25	GENIC	homozygous	50359777
13	51257255	51257256	C	A	10	GENIC	heterozygous	50359779
13	51257839	51257840	C	G	27	GENIC	homozygous	50359781
13	51257975	51257976	C	T	32	GENIC	homozygous	50359783
13	51258041	51258042	C	T	23	GENIC	homozygous	50359784
13	51258379	51258380	C	T	26	GENIC	homozygous	50359786
13	51259469	51259470	T	-	31	GENIC	possibly homozygous	49755844
13	51259889	51259890	G	T	17	GENIC	homozygous	50359788
13	51260075	51260076	T	-	2	GENIC	homozygous	49755845
13	51260078	51260079	T	C	18	GENIC	heterozygous	50359790