chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40695537	40695538	A	G	13	GENIC	homozygous	115328577
12	40695859	40695860	G	A	33	GENIC	homozygous	115328579
12	40695863	40695864	C	T	35	GENIC	homozygous	115328581
12	40696133	40696134	C	A	53	GENIC	homozygous	115328583
12	40696151	40696152	G	A	54	GENIC	homozygous	115328585
12	40696216	40696217	T	C	48	GENIC	homozygous	115328587
12	40696648	40696649	A	T	12	GENIC	homozygous	115328589
12	40696884	40696885	A	T	21	GENIC	homozygous	115328591
12	40697446	40697447	T	C	43	GENIC	homozygous	115328595
12	40697467	40697468	C	T	46	GENIC	homozygous	115328597
12	40698055	40698056	G	A	25	GENIC	possibly homozygous	115328599
12	40699564	40699565	C	A	45	GENIC	homozygous	115328601
12	40699618	40699619	T	C	42	GENIC	homozygous	115328603
12	40700278	40700279	G	T	53	GENIC	homozygous	115328605
12	40700586	40700587	T	C	24	GENIC	homozygous	115515433
12	40700652	40700653	C	G	11	GENIC	homozygous	115383947
12	40701317	40701318	C	A	24	GENIC	homozygous	115328607
12	40701563	40701564	G	A	46	GENIC	homozygous	115328609
12	40705325	40705326	A	G	46	GENIC	homozygous	115328611