chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3406078	3406079	C	T	15	GENIC	possibly homozygous	119756145
20	3406085	3406086	C	T	16	GENIC	heterozygous	119756146
20	3406115	3406116	A	G	15	GENIC	heterozygous	119756147
20	3406125	3406126	C	T	15	GENIC	heterozygous	119756148
20	3406141	3406142	C	T	10	GENIC	heterozygous	119756149
20	3406686	3406687	C	T	31	GENIC	homozygous	109068721
20	3407906	3407907	T	C	22	GENIC	possibly homozygous	109068723
20	3409483	3409484	A	G	16	GENIC	homozygous	109068725
20	3409533	3409534	A	G	23	GENIC	homozygous	109068727
20	3410162	3410163	C	A	20	GENIC	homozygous	109572110
20	3412247	3412248	T	C	24	GENIC	homozygous	109068729
20	3412688	3412689	A	G	30	GENIC	homozygous	109068731
20	3414027	3414028	A	G	19	GENIC	homozygous	109068733
20	3417006	3417007	G	A	21	GENIC	homozygous	109068735
20	3417366	3417367	C	A	29	GENIC	homozygous	109068737
20	3417980	3417981	A	C	14	GENIC	homozygous	109068739
20	3418188	3418189	G	T	24	GENIC	homozygous	109294431