chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41601460	41601461	A	G	19	GENIC	homozygous	115330907
12	41601469	41601470	G	T	20	GENIC	homozygous	115385528
12	41603084	41603085	T	C	31	GENIC	possibly homozygous	115385530
12	41603149	41603150	G	A	33	GENIC	homozygous	115330913
12	41603767	41603768	A	G	18	GENIC	homozygous	115330917
12	41608766	41608767	G	A	30	GENIC	homozygous	115330923
12	41609354	41609355	G	T	26	GENIC	homozygous	115385532
12	41609736	41609737	T	C	23	GENIC	homozygous	115330929
12	41610814	41610815	G	T	20	GENIC	homozygous	115385534
12	41614756	41614757	T	C	39	GENIC	possibly homozygous	118327205
12	41616953	41616954	T	C	23	GENIC	homozygous	115330935
12	41618554	41618555	A	G	29	GENIC	homozygous	115330939
12	41619560	41619561	A	G	44	GENIC	homozygous	115385536