chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	140880529	140880530	T	C	18	GENIC	homozygous	54155940
7	140880530	140880531	T	C	18	GENIC	homozygous	54155942
7	140880619	140880620	C	T	13	GENIC	homozygous	55450438
7	140881143	140881144	A	G	35	GENIC	homozygous	54155944
7	140881222	140881223	G	T	33	GENIC	homozygous	54155946
7	140881227	140881228	C	T	32	GENIC	homozygous	54155948
7	140881237	140881238	A	AGGACCT	29	GENIC	homozygous	54155950
7	140881253	140881254	C	T	27	GENIC	homozygous	54155952
7	140881273	140881274	G	T	32	GENIC	homozygous	54155954
7	140881279	140881280	T	A	30	GENIC	homozygous	54155957
7	140881284	140881285	A	AAATGTGCTGGC	30	GENIC	homozygous	54155959
7	140881298	140881299	T	C	30	GENIC	homozygous	54155961
7	140881299	140881300	G	A	29	GENIC	homozygous	54155963
7	140883657	140883658	G	T	27	GENIC	homozygous	54155965
7	140884300	140884302	TT	--	17	GENIC	possibly homozygous	54155967
7	140886573	140886574	A	AGTCT	24	GENIC	homozygous	54155969
7	140884301	140884302	T	-	17	GENIC	heterozygous	55363312
7	140881239	140881240	G	C	29	GENIC	homozygous	55363310