chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	242798586	242798587	C	A	25	GENIC	homozygous	110344486
2	242798764	242798765	G	T	34	GENIC	homozygous	110344488
2	242800637	242800638	A	G	19	GENIC	homozygous	110344494
2	242800687	242800688	C	T	20	GENIC	homozygous	111187466
2	242801968	242801969	G	C	33	GENIC	homozygous	111187468
2	242802666	242802667	T	G	22	GENIC	homozygous	110344500
2	242804227	242804228	C	T	38	GENIC	homozygous	111187470
2	242805576	242805577	A	G	21	GENIC	homozygous	110344504
2	242806618	242806619	C	T	44	GENIC	homozygous	110344506
2	242818363	242818364	C	A	25	GENIC	homozygous	111187472
2	242821766	242821767	T	A	28	GENIC	homozygous	111187474
2	242822644	242822645	A	G	34	GENIC	homozygous	110344510
2	242825068	242825069	T	G	23	GENIC	homozygous	110344516
2	242825259	242825260	C	T	25	GENIC	possibly homozygous	110344518
2	242825514	242825515	C	T	31	GENIC	possibly homozygous	111187476
2	242826620	242826621	A	G	22	GENIC	homozygous	110344520
2	242828278	242828279	A	G	23	GENIC	homozygous	111187480
2	242828316	242828317	C	G	17	GENIC	homozygous	110344524