chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44256099	44256100	C	A	27	GENIC	homozygous	115336780
12	44256420	44256421	C	T	22	GENIC	homozygous	115336782
12	44257240	44257241	C	T	33	GENIC	homozygous	115390348
12	44257273	44257274	G	C	32	GENIC	homozygous	115336786
12	44257305	44257306	T	G	28	GENIC	homozygous	115336788
12	44257478	44257479	G	A	23	GENIC	homozygous	115336790
12	44258686	44258687	T	C	11	GENIC	homozygous	115336794
12	44261394	44261395	C	A	14	GENIC	homozygous	115390350
12	44263023	44263024	G	A	21	GENIC	homozygous	115390352
12	44265233	44265234	A	G	33	GENIC	homozygous	115390354
12	44265345	44265346	C	T	28	GENIC	possibly homozygous	115336796
12	44267064	44267065	T	G	13	GENIC	homozygous	115390356
12	44268998	44268999	G	A	22	GENIC	homozygous	115390358
12	44271905	44271906	C	T	25	GENIC	homozygous	115390360
12	44274777	44274778	G	A	22	GENIC	homozygous	115430138
12	44274809	44274810	G	A	24	GENIC	homozygous	115390362
12	44275612	44275613	C	T	29	GENIC	homozygous	115486493
12	44275711	44275712	C	T	29	GENIC	homozygous	115390364
12	44276013	44276014	C	T	26	GENIC	homozygous	115336806
12	44276193	44276194	T	C	35	GENIC	homozygous	115390366
12	44276542	44276543	G	A	24	GENIC	homozygous	115336810
12	44276978	44276979	G	A	19	GENIC	homozygous	115336814
12	44277234	44277235	A	C	22	GENIC	homozygous	115336816
12	44278964	44278965	G	C	9	GENIC	homozygous	115336820