chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	10443219	10443220	T	A	41	GENIC	heterozygous	136969763
4	10443244	10443245	G	A	43	GENIC	heterozygous	136969764
4	10443732	10443733	T	C	48	GENIC	heterozygous	136969765
4	10444127	10444128	T	C	46	GENIC	heterozygous	136969766
4	10444543	10444543		GGTCGATGCTTTCTTGGGAAGGGCTTGCTTGCCGGCTGTTGTTCTCAGAGTCTGAATCCTGTAACCACCACATGTGGGGGTTGCTG	43	GENIC	heterozygous	140874115
4	10450404	10450405	G	A	27	GENIC	homozygous	136969767
4	10450943	10450944	G	A	23	GENIC	homozygous	136969768
4	10451446	10451447	C	T	31	GENIC	homozygous	136969769
4	10451515	10451516	G	T	34	GENIC	homozygous	136969770
4	10451524	10451525	G	T	39	GENIC	heterozygous	136969771
4	10451610	10451611	G	C	38	GENIC	heterozygous	136969773
4	10451669	10451670	A	C	32	GENIC	homozygous	136969774
4	10451734	10451735	T	A	30	GENIC	homozygous	136969775