chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40695537	40695538	A	G	3	GENIC	homozygous	115328577
12	40696133	40696134	C	A	23	GENIC	homozygous	115328583
12	40696151	40696152	G	A	29	GENIC	homozygous	115328585
12	40696216	40696217	T	C	28	GENIC	homozygous	115328587
12	40696648	40696649	A	T	38	GENIC	homozygous	115328589
12	40696884	40696885	A	T	21	GENIC	homozygous	115328591
12	40697446	40697447	T	C	29	GENIC	homozygous	115328595
12	40697467	40697468	C	T	32	GENIC	homozygous	115328597
12	40698119	40698120	C	T	14	GENIC	heterozygous	115426796
12	40699564	40699565	C	A	18	GENIC	possibly homozygous	115328601
12	40699618	40699619	T	C	21	GENIC	homozygous	115328603
12	40700278	40700279	G	T	14	GENIC	homozygous	115328605
12	40701317	40701318	C	A	21	GENIC	homozygous	115328607
12	40701563	40701564	G	A	19	GENIC	homozygous	115328609
12	40705325	40705326	A	G	21	GENIC	homozygous	115328611