chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	243052523	243052524	C	T	49	GENIC	possibly homozygous	111032501
2	243053746	243053747	T	C	32	GENIC	homozygous	110913168
2	243054178	243054179	T	G	42	GENIC	homozygous	110913169
2	243054269	243054270	C	A	44	GENIC	homozygous	110913170
2	243057983	243057984	C	A	32	GENIC	homozygous	110633077
2	243059631	243059632	T	G	47	GENIC	possibly homozygous	110913174
2	243060040	243060041	A	C	48	GENIC	homozygous	110345509
2	243060280	243060281	G	A	45	GENIC	homozygous	110345511
2	243061113	243061114	G	A	36	GENIC	homozygous	110345519
2	243061292	243061293	G	A	51	GENIC	homozygous	110345521
2	243061583	243061584	C	T	44	GENIC	homozygous	110845198
2	243061692	243061693	C	T	31	GENIC	homozygous	110345523
2	243062304	243062305	G	A	35	GENIC	homozygous	110345525
2	243062406	243062407	A	G	37	GENIC	homozygous	110345527
2	243062447	243062448	G	C	27	GENIC	heterozygous	111032503
2	243063093	243063094	A	G	38	GENIC	possibly homozygous	110345533
2	243063997	243063998	A	G	45	GENIC	homozygous	110913177
2	243064938	243064939	A	T	30	GENIC	homozygous	110345535
2	243065050	243065051	C	T	46	GENIC	homozygous	110845206
2	243066355	243066356	C	G	44	GENIC	homozygous	110345547
2	243066316	243066317	T	C	45	GENIC	homozygous	110345545
2	243066373	243066374	G	A	39	GENIC	homozygous	110845208