chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	142114411	142114412	A	ATG	37	GENIC	heterozygous	55756749
5	142114412	142114414	CG	--	37	GENIC	heterozygous	55756750
5	142114423	142114424	G	A	42	GENIC	possibly homozygous	55756751
5	142115313	142115315	CA	--	18	GENIC	heterozygous	55756752
5	142115423	142115424	C	CCA	16	GENIC	possibly homozygous	55756753
5	142115512	142115513	T	TACAC	12	GENIC	homozygous	55756754
5	142115580	142115581	C	T	37	GENIC	homozygous	55756755
5	142116406	142116407	G	GT	47	GENIC	homozygous	55756756
5	142116634	142116635	T	A	43	GENIC	homozygous	55756757
5	142116999	142117000	T	A	47	GENIC	homozygous	55756758
5	142117413	142117414	A	C	37	GENIC	homozygous	55756759
5	142118563	142118564	C	T	49	GENIC	homozygous	55756760
5	142118759	142118760	A	G	51	GENIC	homozygous	55756761
5	142118998	142118999	A	G	58	GENIC	homozygous	55756762
5	142119735	142119736	G	A	56	GENIC	homozygous	55756763
5	142120147	142120148	G	A	43	GENIC	possibly homozygous	55756764
5	142120539	142120540	T	C	53	GENIC	homozygous	55756765
5	142120568	142120569	T	C	46	GENIC	homozygous	55756766