chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	46879560	46879561	G	T	38	GENIC	homozygous	115342649
12	46879673	46879674	A	G	17	GENIC	homozygous	115342651
12	46880219	46880220	C	T	42	GENIC	homozygous	115342653
12	46880847	46880848	T	A	26	GENIC	homozygous	115342655
12	46883452	46883453	G	C	43	GENIC	homozygous	115342657
12	46884503	46884504	C	T	35	GENIC	homozygous	115342659
12	46884854	46884855	C	G	27	GENIC	homozygous	115342661
12	46885214	46885215	C	G	29	GENIC	heterozygous	115342663
12	46885758	46885759	C	T	44	GENIC	homozygous	115342665
12	46885889	46885890	T	C	47	GENIC	homozygous	115342667
12	46887085	46887086	G	A	40	GENIC	homozygous	115342669
12	46883715	46883716	G	T	17	GENIC	homozygous	118272517
12	46883754	46883755	T	C	27	GENIC	homozygous	118272518
12	46885189	46885190	C	G	33	GENIC	heterozygous	118272519
12	46885227	46885228	T	C	31	GENIC	heterozygous	118272520
12	46885229	46885230	G	A	31	GENIC	heterozygous	118272521
12	46885234	46885235	C	T	30	GENIC	heterozygous	118272522
12	46888669	46888670	G	C	14	GENIC	heterozygous	118272523
12	46888675	46888676	C	T	15	GENIC	heterozygous	118272524
12	46888705	46888706	A	G	22	GENIC	heterozygous	118272525
12	46889292	46889293	T	C	21	GENIC	homozygous	115342671
12	46889677	46889678	G	A	21	GENIC	homozygous	115342673
12	46889602	46889603	A	G	38	GENIC	possibly homozygous	115480594