chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	252808371	252808372	G	C	17	GENIC	homozygous	108612662
1	252808766	252808767	G	T	20	GENIC	homozygous	109020094
1	252809968	252809968		AAT	16	GENIC	homozygous	132542002
1	252810054	252810055	T	C	19	GENIC	homozygous	109020096
1	252810111	252810111		A	19	GENIC	homozygous	132542003
1	252810211	252810212	A	C	22	GENIC	homozygous	109020097
1	252810225	252810226	T	C	18	GENIC	homozygous	108612664
1	252810307	252810308	G	A	16	GENIC	homozygous	109020098
1	252810315	252810316	T	C	15	GENIC	homozygous	109020099
1	252810360	252810361	G	A	16	GENIC	homozygous	109020100
1	252810444	252810445	A	G	15	GENIC	homozygous	109020101
1	252810590	252810591	A	G	28	GENIC	homozygous	109020102
1	252810796	252810797	C	T	22	GENIC	homozygous	109020103
1	252810934	252810935	T	C	12	GENIC	homozygous	109020104
1	252810971	252810972	A	G	15	GENIC	homozygous	109020105
1	252811000	252811001	G	A	14	GENIC	homozygous	109020106
1	252811030	252811031	C	G	12	GENIC	homozygous	109020107
1	252811092	252811093	G	A	7	GENIC	homozygous	109020108
1	252811142	252811143	G	A	3	GENIC	homozygous	109020109
1	252811182	252811183	G		8	GENIC	homozygous	132542004
1	252811286	252811286		AAAG	10	GENIC	homozygous	132542005
1	252810875	252810876	T	C	11	GENIC	homozygous	120516012
1	252810093	252810094	A		21	GENIC	possibly homozygous	127504327
1	252810874	252810875	C	T	11	GENIC	homozygous	120516011