chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24145156	24145157	A	G	16	GENIC	heterozygous	50131729
12	24145272	24145273	C	T	15	GENIC	heterozygous	50131731
12	24145307	24145308	G	A	16	GENIC	heterozygous	50131733
12	24145821	24145822	G	C	15	GENIC	heterozygous	50131737
12	24146241	24146242	T	G	23	GENIC	heterozygous	50131741
12	24146384	24146385	A	G	23	GENIC	heterozygous	50131743
12	24146490	24146491	G	A	21	GENIC	heterozygous	50131745
12	24146698	24146699	C	T	24	GENIC	heterozygous	50131753
12	24146812	24146813	C	T	32	GENIC	heterozygous	50131755
12	24147143	24147144	C	T	10	GENIC	heterozygous	50131759
12	24147255	24147256	G	C	12	GENIC	heterozygous	50131763
12	24147437	24147438	C	T	13	GENIC	heterozygous	50131765
12	24147506	24147507	A	G	16	GENIC	heterozygous	50131767
12	24147980	24147981	G	A	46	GENIC	heterozygous	50131769
12	24150796	24150797	A	G	8	GENIC	heterozygous	50131806
12	24151460	24151461	A	G	10	GENIC	heterozygous	50131812
12	24153249	24153250	A	G	13	GENIC	heterozygous	50131831
12	24153572	24153573	G	T	12	GENIC	heterozygous	50131835
12	24153724	24153725	C	T	18	GENIC	heterozygous	50131837
12	24154251	24154252	A	G	16	GENIC	heterozygous	50131841
12	24154845	24154846	C	T	10	GENIC	heterozygous	51230589
12	24155606	24155607	T	C	28	GENIC	heterozygous	50131851