chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	129795360	129795361	T	C	3	GENIC	homozygous	54109587
7	129795406	129795407	A	-	17	GENIC	possibly homozygous	54241221
7	129796093	129796094	A	T	26	GENIC	homozygous	54109589
7	129796800	129796803	ACC	---	9	GENIC	heterozygous	55632335
7	129796801	129796803	CC	--	9	GENIC	heterozygous	54109590
7	129797073	129797074	G	A	27	GENIC	homozygous	54109591
7	129798576	129798577	A	AAAGC	5	GENIC	homozygous	54109592
7	129795959	129795960	T	TTGGG	1	GENIC	homozygous	55010199
7	129795961	129795962	A	ATTTAGCTCAGTGGTAGAGCGCTTGCCTAG	1	GENIC	homozygous	55010201
7	129796802	129796803	C	-	9	GENIC	heterozygous	55010203
7	129800366	129800367	T	-	19	GENIC	homozygous	54754231
7	129800826	129800827	C	CAT	21	GENIC	homozygous	54109594
7	129801567	129801568	G	-	8	GENIC	possibly homozygous	54109596
7	129802532	129802533	T	C	23	GENIC	homozygous	54109597
7	129803707	129803708	T	A	33	GENIC	homozygous	54109598
7	129803754	129803755	A	C	22	GENIC	homozygous	54109599
7	129804462	129804465	CAC	---	13	GENIC	homozygous	54109600
7	129799664	129799665	C	T	30	GENIC	homozygous	55879691
7	129801566	129801568	GG	--	8	GENIC	heterozygous	54676888