chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	29447287	29447288	T	C	71	GENIC	homozygous	109159801
20	29450098	29450099	A	G	46	GENIC	homozygous	109159809
20	29450564	29450565	A	G	27	GENIC	homozygous	109159811
20	29451484	29451485	C	T	54	GENIC	homozygous	109250710
20	29452732	29452733	G	C	40	GENIC	homozygous	109250712
20	29453273	29453274	T	C	56	GENIC	homozygous	109159817
20	29453525	29453526	C	T	46	GENIC	homozygous	109159819
20	29453787	29453788	G	A	53	GENIC	homozygous	109159821
20	29454418	29454419	C	T	25	GENIC	homozygous	109159823
20	29455522	29455523	C	T	77	GENIC	homozygous	109159825
20	29455528	29455529	G	A	75	GENIC	homozygous	109250714
20	29455809	29455810	C	T	34	GENIC	homozygous	109250716
20	29456392	29456393	G	C	31	GENIC	homozygous	109159827
20	29457259	29457260	G	A	29	GENIC	homozygous	109250718
20	29457774	29457775	G	A	49	GENIC	homozygous	109250720
20	29461638	29461639	A	G	33	GENIC	possibly homozygous	109159831
20	29462774	29462775	C	T	45	GENIC	homozygous	109310547
20	29462837	29462838	C	T	66	GENIC	homozygous	109250724
20	29463413	29463414	G	A	5	GENIC	homozygous	109159835