chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3991065	3991066	T	G	42	GENIC	homozygous	109070779
20	3991123	3991124	A	G	34	GENIC	homozygous	109070785
20	3991316	3991317	G	C	46	GENIC	homozygous	109070793
20	3991427	3991428	C	T	56	GENIC	homozygous	109070799
20	3991769	3991770	A	C	42	GENIC	possibly homozygous	109389229
20	3991838	3991839	C	G	40	GENIC	homozygous	109389230
20	3991882	3991883	C	A	35	GENIC	homozygous	109389231
20	3992273	3992274	A	C	22	GENIC	homozygous	131559241
20	3992302	3992302		A	19	GENIC	homozygous	131554686
20	3992425	3992426	C	T	14	GENIC	homozygous	131559242
20	3992698	3992699	C	T	13	GENIC	homozygous	129706123
20	3992798	3992799	C	A	3	GENIC	homozygous	129706125
20	3992800	3992801	G	T	3	GENIC	homozygous	131559243
20	3992869	3992870	G	C	2	GENIC	homozygous	129706128