chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3553906	3553907	C	T	11	GENIC	homozygous	109069050
20	3554097	3554098	T	G	12	GENIC	homozygous	109069052
20	3557013	3557014	C	T	5	GENIC	homozygous	109069054
20	3557322	3557323	G	T	6	GENIC	homozygous	109069056
20	3557368	3557369	C	T	8	GENIC	homozygous	109069058
20	3557546	3557547	A	T	4	GENIC	homozygous	109069060
20	3558080	3558081	T	C	23	GENIC	homozygous	109069062
20	3558518	3558519	G	A	15	GENIC	homozygous	109069064
20	3561290	3561291	C	T	19	GENIC	homozygous	109069068
20	3561391	3561392	A	G	21	GENIC	homozygous	109069070
20	3562750	3562751	C	T	10	GENIC	homozygous	109069072
20	3562751	3562752	C	T	10	GENIC	homozygous	109069074
20	3564434	3564435	T	C	18	GENIC	homozygous	109069076
20	3564691	3564692	C	T	11	GENIC	homozygous	109069078
20	3565716	3565717	C	T	15	GENIC	homozygous	109328521
20	3567270	3567271	G	A	6	GENIC	homozygous	109069080
20	3567637	3567638	A	G	4	GENIC	homozygous	109069082
20	3568323	3568324	T	G	14	GENIC	homozygous	109069084
20	3570271	3570272	T	C	13	GENIC	homozygous	109069086
20	3570393	3570394	A	G	10	GENIC	homozygous	109069088
20	3573009	3573010	T	G	7	GENIC	homozygous	109069090
20	3573300	3573301	C	A	20	GENIC	homozygous	109069092
20	3573647	3573648	G	A	21	GENIC	homozygous	109069095
20	3573929	3573930	C	T	15	GENIC	homozygous	109069097
20	3574212	3574213	C	T	6	GENIC	homozygous	109069099
20	3565714	3565715	G	T	15	GENIC	homozygous	109477541