chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39654050	39654051	G	A	36	GENIC	homozygous	115326409
12	39654243	39654244	C	A	42	GENIC	homozygous	115326411
12	39654446	39654447	C	T	33	GENIC	homozygous	115326413
12	39655684	39655685	C	T	42	GENIC	homozygous	115326415
12	39656622	39656623	T	C	32	GENIC	homozygous	115326419
12	39656655	39656656	G	A	31	GENIC	homozygous	115326421
12	39656677	39656678	C	G	32	GENIC	homozygous	115326423
12	39656691	39656692	G	A	32	GENIC	homozygous	115326425
12	39657329	39657330	C	T	35	GENIC	homozygous	115326427
12	39657635	39657636	A	G	39	GENIC	homozygous	115326429
12	39658541	39658542	A	C	28	GENIC	homozygous	115326431
12	39658918	39658919	C	T	52	GENIC	homozygous	115326433
12	39659443	39659444	A	G	31	GENIC	homozygous	115326435
12	39660496	39660497	T	C	23	GENIC	homozygous	115326437
12	39661341	39661342	G	A	30	GENIC	homozygous	115326439
12	39662949	39662950	G	A	17	GENIC	homozygous	115326441
12	39663840	39663841	G	A	30	GENIC	homozygous	115326443
12	39665596	39665597	T	C	38	GENIC	homozygous	115326445
12	39667542	39667543	A	G	22	GENIC	homozygous	115326447
12	39667800	39667801	A	G	28	GENIC	homozygous	115326449