chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	143909402	143909403	T	C	23	GENIC	homozygous	115944782
7	143909478	143909479	T	C	35	GENIC	homozygous	115944783
7	143913006	143913007	A	G	37	GENIC	homozygous	115944785
7	143913815	143913816	A	G	43	GENIC	homozygous	115944786
7	143915316	143915317	G	A	30	GENIC	homozygous	116396852
7	143916266	143916267	C	G	46	GENIC	homozygous	116396853
7	143917014	143917015	C	T	25	GENIC	possibly homozygous	116396854
7	143918312	143918313	C	T	39	GENIC	homozygous	116396855
7	143918685	143918686	G	A	27	GENIC	homozygous	116396856
7	143919524	143919525	C	A	17	GENIC	homozygous	116396857
7	143919526	143919527	G	A	18	GENIC	homozygous	116396858
7	143919527	143919528	G	A	18	GENIC	homozygous	116396859
7	143919756	143919757	A	T	23	GENIC	homozygous	116396860
7	143920297	143920298	C	T	35	GENIC	homozygous	116396862
7	143920515	143920516	A	G	28	GENIC	homozygous	116396863
7	143921297	143921298	C	G	20	GENIC	homozygous	116396864
7	143922559	143922560	C	T	37	GENIC	homozygous	116396865
7	143923032	143923033	T	G	32	GENIC	homozygous	116396866