chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	121212800	121212801	C	T	29	GENIC	homozygous	108922101
1	121213418	121213419	G	T	25	GENIC	homozygous	108922102
1	121213631	121213632	A	G	37	GENIC	homozygous	108922104
1	121213705	121213706	T	C	40	GENIC	homozygous	108922105
1	121213746	121213747	A	G	30	GENIC	homozygous	108922106
1	121213868	121213869	G	A	31	GENIC	homozygous	108922107
1	121213904	121213905	A	T	27	GENIC	homozygous	108922108
1	121214574	121214575	G	T	24	GENIC	homozygous	108922114
1	121214735	121214736	A	G	32	GENIC	homozygous	108922115
1	121214772	121214773	A	C	34	GENIC	homozygous	108922116
1	121215077	121215078	C	T	43	GENIC	homozygous	108922117
1	121215220	121215221	C	G	30	GENIC	homozygous	108922118
1	121216594	121216595	T	C	30	GENIC	homozygous	108922136
1	121216889	121216890	A	C	39	GENIC	homozygous	108922137
1	121216992	121216993	A	T	43	GENIC	possibly homozygous	108922138
1	121217078	121217079	C	G	36	GENIC	homozygous	108922139
1	121217259	121217260	T	C	19	GENIC	homozygous	108922140
1	121217340	121217341	A	T	26	GENIC	homozygous	108202584
1	121217381	121217382	A	G	29	GENIC	homozygous	108202585
1	121217457	121217458	C	T	30	GENIC	homozygous	108922141
1	121217521	121217522	A	T	31	GENIC	homozygous	108922142
1	121217971	121217972	G	A	39	GENIC	homozygous	108922143
1	121218041	121218042	G	A	39	GENIC	homozygous	108922144