chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	107330102	107330103	C	T	21	GENIC	homozygous	119401771
4	107330310	107330311	A	C	5	GENIC	homozygous	119401775
4	107330390	107330391	G	T	20	GENIC	homozygous	119401777
4	107330471	107330472	T	C	16	GENIC	homozygous	119401779
4	107330660	107330661	T	G	20	GENIC	possibly homozygous	119401781
4	107330860	107330861	T	C	13	GENIC	homozygous	119401783
4	107331825	107331826	G	T	10	GENIC	homozygous	113549280
4	107331881	107331882	A	G	15	GENIC	homozygous	119401785
4	107332316	107332317	A	G	13	GENIC	homozygous	119401787
4	107332769	107332770	C	T	18	GENIC	homozygous	113549284
4	107333082	107333083	C	T	7	GENIC	homozygous	119401789
4	107331792	107331793	C	A	14	GENIC	homozygous	119586520
4	107333542	107333543	G	T	16	GENIC	homozygous	113549290
4	107333873	107333874	G	C	20	GENIC	homozygous	119401791
4	107334201	107334202	T	C	9	GENIC	homozygous	113549292
4	107334465	107334466	T	C	10	GENIC	homozygous	113549294
4	107336179	107336180	T	C	22	GENIC	homozygous	113549302
4	107336316	107336317	C	T	15	GENIC	homozygous	119401793
4	107337647	107337648	G	T	10	GENIC	homozygous	119401795
4	107338173	107338174	G	A	10	GENIC	heterozygous	119401797
4	107338342	107338343	T	C	11	GENIC	homozygous	113549310
4	107338705	107338706	G	A	20	GENIC	homozygous	119401799
4	107339302	107339303	C	G	10	GENIC	homozygous	113549318
4	107339395	107339396	C	A	16	GENIC	homozygous	119401801
4	107339856	107339857	T	C	16	GENIC	homozygous	119401803
4	107340079	107340080	T	C	4	GENIC	homozygous	119401805
4	107340370	107340371	G	A	21	GENIC	homozygous	119401807