chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40695537	40695538	A	G	20	GENIC	homozygous	115328577
12	40695859	40695860	G	A	16	GENIC	homozygous	115328579
12	40695863	40695864	C	T	16	GENIC	homozygous	115328581
12	40696133	40696134	C	A	17	GENIC	homozygous	115328583
12	40696151	40696152	G	A	18	GENIC	homozygous	115328585
12	40696216	40696217	T	C	23	GENIC	homozygous	115328587
12	40696648	40696649	A	T	14	GENIC	homozygous	115328589
12	40696884	40696885	A	T	26	GENIC	homozygous	115328591
12	40697020	40697021	A	C	11	GENIC	homozygous	115328593
12	40697446	40697447	T	C	16	GENIC	homozygous	115328595
12	40697467	40697468	C	T	15	GENIC	homozygous	115328597
12	40697524	40697525	C	A	19	GENIC	homozygous	115383945
12	40700278	40700279	G	T	27	GENIC	homozygous	115328605
12	40701317	40701318	C	A	20	GENIC	homozygous	115328607
12	40701563	40701564	G	A	22	GENIC	homozygous	115328609
12	40705325	40705326	A	G	21	GENIC	homozygous	115328611
12	40706564	40706565	T	G	30	GENIC	homozygous	115383949
12	40706860	40706861	T	G	33	GENIC	homozygous	115383951
12	40707289	40707290	C	T	34	GENIC	homozygous	115494878
12	40707476	40707477	C	T	21	GENIC	homozygous	115383953