chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	141246476	141246477	T	C	30	GENIC	homozygous	69180442
7	141246502	141246503	C	A	28	GENIC	homozygous	69180443
7	141247268	141247269	C	T	31	GENIC	homozygous	69180444
7	141247856	141247857	G	A	43	GENIC	homozygous	69180445
7	141247891	141247892	T	G	40	GENIC	possibly homozygous	69180446
7	141248371	141248372	T	A	41	GENIC	homozygous	69180447
7	141248480	141248481	C	A	35	GENIC	homozygous	69180448
7	141249540	141249541	C	T	32	GENIC	homozygous	69180455
7	141250499	141250500	T	C	33	GENIC	homozygous	69180456
7	141250806	141250807	A	G	36	GENIC	homozygous	69180457
7	141250944	141250945	A	G	42	GENIC	homozygous	69180458