chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	227429473	227429474	G	C	14	GENIC	homozygous	108559218
1	227429643	227429644	A	C	25	GENIC	homozygous	108559219
1	227430046	227430047	T	C	16	GENIC	homozygous	108559220
1	227430337	227430338	T	C	15	GENIC	possibly homozygous	108559221
1	227430355	227430356	C	T	17	GENIC	possibly homozygous	108559222
1	227430385	227430386	C	T	16	GENIC	possibly homozygous	108559223
1	227430596	227430597	A	G	53	GENIC	homozygous	108559224
1	227430721	227430722	A	G	43	GENIC	homozygous	108559225
1	227430729	227430730	A	G	45	GENIC	homozygous	108559226
1	227430874	227430875	A	G	29	GENIC	homozygous	108559227
1	227431045	227431046	T	C	28	GENIC	homozygous	108559228
1	227431460	227431461	C	A	60	GENIC	homozygous	108559229
1	227431634	227431635	T	C	13	GENIC	homozygous	108559230
1	227431795	227431796	A	T	24	GENIC	homozygous	108559231
1	227432241	227432242	T	C	26	GENIC	homozygous	108559233
1	227432281	227432282	G	C	29	GENIC	homozygous	108559234
1	227432968	227432969	G	T	33	GENIC	homozygous	108559235
1	227434502	227434503	G	A	23	GENIC	homozygous	108559239
1	227437038	227437039	T	C	20	GENIC	homozygous	108559244
1	227438251	227438252	T	G	22	GENIC	homozygous	120876666
1	227438284	227438285	A	G	23	GENIC	homozygous	120876667
1	227438289	227438290	G	T	22	GENIC	homozygous	120876668
1	227438682	227438683	G	A	35	GENIC	homozygous	120876669
1	227439268	227439269	A	T	29	GENIC	homozygous	108559247
1	227439848	227439849	C	T	32	GENIC	homozygous	120876670