chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	243053746	243053747	T	C	28	GENIC	homozygous	110913168
2	243054178	243054179	T	G	32	GENIC	homozygous	110913169
2	243054269	243054270	C	A	34	GENIC	homozygous	110913170
2	243055581	243055582	A	G	21	GENIC	homozygous	110913171
2	243057145	243057146	G	A	21	GENIC	homozygous	110913172
2	243059458	243059459	T	C	36	GENIC	homozygous	110913173
2	243059631	243059632	T	G	37	GENIC	homozygous	110913174
2	243059997	243059998	C	T	35	GENIC	homozygous	110913175
2	243060040	243060041	A	C	40	GENIC	homozygous	110345509
2	243060280	243060281	G	A	30	GENIC	homozygous	110345511
2	243062304	243062305	G	A	16	GENIC	homozygous	110345525
2	243063093	243063094	A	G	24	GENIC	homozygous	110345533
2	243063997	243063998	A	G	17	GENIC	homozygous	110913177
2	243066141	243066142	T	C	47	GENIC	homozygous	120272804
2	243066143	243066144	C	T	45	GENIC	homozygous	120181796
2	243066316	243066317	T	C	29	GENIC	possibly homozygous	110345545
2	243066355	243066356	C	G	31	GENIC	homozygous	110345547
2	243066373	243066374	G	A	30	GENIC	homozygous	110845208