chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61460385	61460386	T	-	8	GENIC	heterozygous	51670503
10	61466219	61466220	G	GT	23	GENIC	homozygous	51470876
10	61469728	61469729	T	-	5	GENIC	heterozygous	52379979
10	61486285	61486286	G	GTT	5	GENIC	heterozygous	52379981
10	61486286	61486287	T	-	5	GENIC	heterozygous	52601695
10	61533510	61533512	GC	--	28	GENIC	homozygous	52319782
10	61533514	61533516	GC	--	26	GENIC	homozygous	52319784
10	61533517	61533518	T	TAA	24	GENIC	homozygous	52379985
10	61533519	61533520	A	T	25	GENIC	homozygous	52379987
10	61533521	61533522	G	GAAA	27	GENIC	homozygous	52379989
10	61533523	61533524	C	A	28	GENIC	homozygous	52379991
10	61533533	61533534	T	G	28	GENIC	homozygous	51470890
10	61533557	61533558	G	C	24	GENIC	homozygous	51470891
10	61533558	61533559	A	T	25	GENIC	homozygous	51470892
10	61533562	61533563	C	T	23	GENIC	homozygous	51470893
10	61533563	61533564	A	T	24	GENIC	homozygous	51470894
10	61533567	61533568	G	A	24	GENIC	homozygous	51470895
10	61533570	61533571	C	T	24	GENIC	homozygous	51470896
10	61533578	61533579	T	A	23	GENIC	homozygous	52379993
10	61533580	61533583	TTC	---	28	GENIC	homozygous	52379995
10	61533584	61533585	T	TGAA	27	GENIC	homozygous	52379997
10	61533587	61533588	C	T	27	GENIC	homozygous	51470897
10	61533687	61533688	G	GCCTGGAGCTTCATTCTCCCTTGGCTCTT	28	GENIC	homozygous	52379999
10	61533689	61533690	A	G	28	GENIC	homozygous	52380001
10	61546108	61546109	C	CA	29	GENIC	homozygous	51470903
10	61567916	61567917	G	T	27	GENIC	homozygous	51470913