chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40695537	40695538	A	G	5	GENIC	homozygous	115328577
12	40695859	40695860	G	A	10	GENIC	homozygous	115328579
12	40695863	40695864	C	T	10	GENIC	homozygous	115328581
12	40696151	40696152	G	A	15	GENIC	homozygous	115328585
12	40696216	40696217	T	C	17	GENIC	homozygous	115328587
12	40696648	40696649	A	T	12	GENIC	homozygous	115328589
12	40696884	40696885	A	T	8	GENIC	homozygous	115328591
12	40697279	40697280	A	T	4	GENIC	homozygous	126245460
12	40697446	40697447	T	C	14	GENIC	homozygous	115328595
12	40697467	40697468	C	T	20	GENIC	homozygous	115328597
12	40699296	40699297	T	C	20	GENIC	homozygous	126245461
12	40700586	40700587	T	C	6	GENIC	heterozygous	115515433
12	40701317	40701318	C	A	21	GENIC	homozygous	115328607
12	40702959	40702960	T	C	11	GENIC	homozygous	115441628
12	40705325	40705326	A	G	6	GENIC	homozygous	115328611
12	40706860	40706861	T	G	11	GENIC	homozygous	115383951
12	40707476	40707477	C	T	15	GENIC	homozygous	115383953
12	40707694	40707695	C	T	29	GENIC	homozygous	126245462
12	40709230	40709231	G	A	22	GENIC	homozygous	126245463