chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	274245290	274245291	C	T	22	GENIC	homozygous	108654239
1	274245513	274245514	G	T	26	GENIC	homozygous	108654241
1	274247017	274247018	T	C	46	GENIC	homozygous	108654243
1	274247432	274247433	G	A	34	GENIC	homozygous	108654245
1	274248132	274248133	G	A	39	GENIC	homozygous	108654246
1	274248379	274248380	C	A	21	GENIC	homozygous	108654248
1	274249342	274249343	T	C	42	GENIC	homozygous	108654250
1	274249538	274249539	A	G	22	GENIC	homozygous	108654252
1	274249982	274249983	G	A	28	GENIC	homozygous	108654253
1	274250089	274250090	C	T	29	GENIC	homozygous	108654255
1	274250098	274250099	G	A	33	GENIC	homozygous	108654257
1	274250503	274250504	G	T	7	GENIC	homozygous	108654258
1	274250546	274250547	G	C	7	GENIC	homozygous	108654260
1	274250610	274250611	T	C	18	GENIC	homozygous	108654262
1	274253088	274253089	C	T	27	GENIC	heterozygous	108654263
1	274254807	274254808	A	G	30	GENIC	homozygous	108654265
1	274257057	274257058	T	C	31	GENIC	homozygous	108654266
1	274257513	274257514	G	C	46	GENIC	homozygous	108654268
1	274258420	274258421	A	G	47	GENIC	homozygous	108654269