chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	22717336	22717337	G	C	22	GENIC	possibly homozygous	118261504
12	22717346	22717347	C	T	21	GENIC	homozygous	118261505
12	22717366	22717367	T	C	33	GENIC	heterozygous	118261506
12	22717367	22717368	T	C	33	GENIC	possibly homozygous	115484235
12	22717380	22717381	C	T	33	GENIC	heterozygous	118261507
12	22717382	22717383	C	T	29	GENIC	homozygous	118261508
12	22717508	22717509	G	A	37	GENIC	possibly homozygous	115282630
12	22717724	22717725	A	G	77	GENIC	heterozygous	118261509
12	22717788	22717789	G	A	44	GENIC	heterozygous	118261510
12	22717803	22717804	G	A	37	GENIC	heterozygous	118261511
12	22717922	22717923	C	T	36	GENIC	homozygous	115282632
12	22717925	22717926	G	A	35	GENIC	homozygous	115282634
12	22718621	22718622	A	G	58	GENIC	homozygous	115282636
12	22718743	22718744	C	T	52	GENIC	homozygous	115282638
12	22719047	22719048	T	C	53	GENIC	homozygous	115282640
12	22720179	22720180	A	G	54	GENIC	homozygous	115282642
12	22721030	22721031	A	G	69	GENIC	homozygous	115282644
12	22722494	22722495	A	G	35	GENIC	homozygous	115282646
12	22722767	22722768	A	C	44	GENIC	homozygous	115282648
12	22722957	22722958	G	A	54	GENIC	possibly homozygous	115282650
12	22723868	22723869	T	A	42	GENIC	homozygous	115282652
12	22724955	22724956	A	C	68	GENIC	heterozygous	118261512
12	22725004	22725005	C	T	57	GENIC	heterozygous	118261513
12	22725051	22725052	C	A	36	GENIC	possibly homozygous	118261514
12	22725058	22725059	C	T	40	GENIC	homozygous	118261515
12	22725389	22725390	G	A	50	GENIC	homozygous	115282654
12	22725418	22725419	G	T	48	GENIC	homozygous	115282656
12	22726689	22726690	C	T	43	GENIC	homozygous	115282658