chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51240525	51240527	GG	--	14	GENIC	homozygous	50517724
13	51245854	51245855	A	-	8	GENIC	homozygous	50517726
13	51252109	51252110	G	GCACACA	14	GENIC	homozygous	50836166
13	51254907	51254908	G	A	11	GENIC	homozygous	50359767
13	51242890	51242894	TGTC	----	5	GENIC	homozygous	50359750
13	51244642	51244643	A	-	14	GENIC	homozygous	50359752
13	51245764	51245765	G	A	13	GENIC	homozygous	50359754
13	51250508	51250509	A	G	22	GENIC	homozygous	50359757
13	51251429	51251430	T	G	15	GENIC	homozygous	50359759
13	51254404	51254405	C	T	12	GENIC	homozygous	50359763
13	51254857	51254858	A	C	19	GENIC	homozygous	50359765
13	51242278	51242282	AGAG	----	2	GENIC	homozygous	50602184
13	51245324	51245325	C	CTGTGTGTGTG	6	GENIC	homozygous	50612454
13	51255289	51255290	T	C	5	GENIC	homozygous	50359769
13	51255944	51255958	TTGAACTTCTGACC	--------------	4	GENIC	homozygous	50359771
13	51256033	51256034	C	T	4	GENIC	homozygous	50359773
13	51256311	51256312	G	A	11	GENIC	homozygous	50359775
13	51256344	51256345	T	C	9	GENIC	homozygous	50359777
13	51257839	51257840	C	G	33	GENIC	homozygous	50359781
13	51257975	51257976	C	T	21	GENIC	homozygous	50359783
13	51258041	51258042	C	T	14	GENIC	homozygous	50359784
13	51258379	51258380	C	T	24	GENIC	homozygous	50359786
13	51257237	51257238	A	ATATATGATATATAGTATATGCTATCTATATCTATATC	6	GENIC	homozygous	51064325
13	51259469	51259470	T	-	20	GENIC	possibly homozygous	49755844
13	51259889	51259890	G	T	7	GENIC	homozygous	50359788
13	51257227	51257228	C	CATAT	7	GENIC	homozygous	51064322