chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	243053746	243053747	T	C	4	GENIC	homozygous	110913168
2	243054269	243054270	C	A	25	GENIC	homozygous	110913170
2	243055581	243055582	A	G	8	GENIC	homozygous	110913171
2	243057145	243057146	G	A	18	GENIC	homozygous	110913172
2	243059458	243059459	T	C	22	GENIC	homozygous	110913173
2	243059631	243059632	T	G	12	GENIC	homozygous	110913174
2	243059997	243059998	C	T	20	GENIC	homozygous	110913175
2	243060040	243060041	A	C	13	GENIC	homozygous	110345509
2	243060280	243060281	G	A	20	GENIC	homozygous	110345511
2	243061583	243061584	C	T	16	GENIC	homozygous	110845198
2	243057983	243057984	C	A	7	GENIC	homozygous	110633077
2	243061113	243061114	G	A	14	GENIC	homozygous	110345519
2	243061292	243061293	G	A	28	GENIC	homozygous	110345521
2	243062304	243062305	G	A	17	GENIC	homozygous	110345525
2	243062406	243062407	A	G	23	GENIC	homozygous	110345527
2	243061548	243061549	A	T	5	GENIC	homozygous	125674061
2	243063093	243063094	A	G	19	GENIC	homozygous	110345533
2	243063997	243063998	A	G	19	GENIC	homozygous	110913177
2	243066316	243066317	T	C	17	GENIC	homozygous	110345545
2	243066355	243066356	C	G	14	GENIC	homozygous	110345547
2	243066373	243066374	G	A	12	GENIC	homozygous	110845208