chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	53110842	53110842		A	10	GENIC	heterozygous	132510255
18	53110844	53110848	AGCT		10	GENIC	heterozygous	135378973
18	53120234	53120235	C	T	34	GENIC	heterozygous	135381113
18	53197930	53197931	T	C	31	GENIC	heterozygous	110351765
18	53200555	53200556	C		13	GENIC	homozygous	129539074
18	53204358	53204358		A	9	GENIC	homozygous	129539075
18	53204365	53204367	TA		9	GENIC	homozygous	129539076
18	53204465	53204466	T		19	GENIC	homozygous	129539077
18	53204634	53204634		T	3	GENIC	homozygous	129539078
18	53209843	53209843		A	6	GENIC	homozygous	129539079
18	53209851	53209852	T		7	GENIC	homozygous	129539080
18	53209859	53209860	C		8	GENIC	homozygous	129539081
18	53209968	53209969	G		16	GENIC	homozygous	129539082
18	53210014	53210015	G		14	GENIC	homozygous	129539083
18	53210022	53210022		A	13	GENIC	homozygous	129539084
18	53210033	53210033		C	11	GENIC	homozygous	129539085
18	53210155	53210156	C		15	GENIC	homozygous	129539086
18	53210416	53210417	T	C	13	GENIC	homozygous	110351777
18	53210420	53210421	C	A	10	GENIC	homozygous	110351779
18	53223154	53223155	A		9	GENIC	homozygous	129539107
18	53210165	53210165		G	17	GENIC	homozygous	129539087
18	53210222	53210222		AT	17	GENIC	homozygous	129539088
18	53210373	53210374	T		14	GENIC	homozygous	129539089
18	53210380	53210380		T	14	GENIC	homozygous	129539090
18	53210438	53210439	G		10	GENIC	homozygous	129539091
18	53213876	53213876		G	13	GENIC	homozygous	129539102
18	53213921	53213921		A	17	GENIC	homozygous	129539103
18	53223136	53223137	A		10	GENIC	homozygous	129539105
18	53223144	53223145	A		9	GENIC	homozygous	129539106
18	53231276	53231277	A		16	GENIC	homozygous	129539112
18	53256231	53256232	A	C	13	GENIC	heterozygous	133036336