chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	29447287	29447288	T	C	46	GENIC	homozygous	109159801
20	29448144	29448145	A	C	31	GENIC	homozygous	109434620
20	29450098	29450099	A	G	49	GENIC	homozygous	109159809
20	29450564	29450565	A	G	30	GENIC	homozygous	109159811
20	29451484	29451485	C	T	30	GENIC	homozygous	109250710
20	29452732	29452733	G	C	46	GENIC	homozygous	109250712
20	29453273	29453274	T	C	32	GENIC	homozygous	109159817
20	29453525	29453526	C	T	34	GENIC	homozygous	109159819
20	29453787	29453788	G	A	31	GENIC	homozygous	109159821
20	29454418	29454419	C	T	33	GENIC	homozygous	109159823
20	29455522	29455523	C	T	27	GENIC	homozygous	109159825
20	29455528	29455529	G	A	24	GENIC	homozygous	109250714
20	29455809	29455810	C	T	27	GENIC	homozygous	109250716
20	29456392	29456393	G	C	36	GENIC	homozygous	109159827
20	29457259	29457260	G	A	38	GENIC	homozygous	109250718
20	29461638	29461639	A	G	22	GENIC	homozygous	109159831
20	29462837	29462838	C	T	33	GENIC	homozygous	109250724
20	29463413	29463414	G	A	14	GENIC	homozygous	109159835
20	29462774	29462775	C	T	27	GENIC	homozygous	109310547