chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	276691336	276691337	G	T	29	GENIC	homozygous	108659246
1	276691342	276691343	G	C	29	GENIC	homozygous	108659247
1	276697393	276697394	A	G	20	GENIC	homozygous	108659249
1	276697861	276697862	A	G	16	GENIC	homozygous	108659250
1	276700789	276700790	T	C	34	GENIC	homozygous	108659251
1	276701347	276701348	T	G	20	GENIC	homozygous	108659252
1	276702945	276702946	T	A	30	GENIC	homozygous	108659253
1	276705492	276705493	G	T	19	GENIC	homozygous	108659254
1	276710202	276710203	T	C	16	GENIC	homozygous	120477626
1	276710203	276710204	C	T	16	GENIC	homozygous	109221110
1	276713258	276713259	G	C	32	GENIC	homozygous	108659258
1	276715216	276715217	C	T	38	GENIC	homozygous	108659260
1	276715609	276715610	G	A	9	GENIC	homozygous	108804252
1	276718914	276718915	G	A	21	GENIC	homozygous	108659261
1	276719582	276719583	A	G	35	GENIC	homozygous	108659262
1	276719839	276719840	G	A	40	GENIC	homozygous	108659263
1	276723194	276723195	A	G	22	GENIC	homozygous	108659267
1	276724995	276724996	T	C	29	GENIC	homozygous	108659268
1	276727355	276727356	A	G	23	GENIC	homozygous	108659271
1	276729368	276729369	T	G	27	GENIC	homozygous	108659272