chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	216715528	216715528		A	24	GENIC	possibly homozygous	131782167
1	216722415	216722416	C	T	49	GENIC	homozygous	108991948
1	216719033	216719034	A	G	44	GENIC	homozygous	108991945
1	216720832	216720833	C	T	41	GENIC	homozygous	108991946
1	216721458	216721459	A	C	42	GENIC	homozygous	108991947
1	216722669	216722671	AT		35	GENIC	homozygous	130832764
1	216729768	216729769	A	T	45	GENIC	homozygous	108991949
1	216730099	216730100	A	G	44	GENIC	homozygous	108991950
1	216731239	216731239		A	38	GENIC	possibly homozygous	131782168
1	216732424	216732425	A		27	GENIC	heterozygous	130621138
1	216732990	216732991	T	G	46	GENIC	homozygous	108991951
1	216734141	216734142	A	G	53	GENIC	homozygous	108991952
1	216734684	216734684		A	31	GENIC	possibly homozygous	131782169
1	216736223	216736224	T	C	38	GENIC	homozygous	108991953
1	216737143	216737144	T	C	47	GENIC	homozygous	108991954
1	216737590	216737591	T	C	47	GENIC	homozygous	108991955
1	216742218	216742219	A	G	52	GENIC	homozygous	108991956
1	216742443	216742446	AAC		35	GENIC	homozygous	131782171
1	216744245	216744246	C	G	54	GENIC	homozygous	108991957
1	216745396	216745404	AAAAAAAG		41	GENIC	homozygous	131782172
1	216750191	216750192	C	T	59	GENIC	homozygous	108991958