chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12071850	12071851	T	TA	28	GENIC	homozygous	45430122
20	12072354	12072355	C	T	48	GENIC	possibly homozygous	45430131
20	12072589	12072590	C	G	45	GENIC	homozygous	45684809
20	12072655	12072656	G	A	54	GENIC	homozygous	45684810
20	12072708	12072709	C	A	57	GENIC	homozygous	45430138
20	12072847	12072848	T	C	62	GENIC	homozygous	45430139
20	12072900	12072901	C	T	43	GENIC	homozygous	45684811
20	12072929	12072930	C	T	43	GENIC	possibly homozygous	45684812
20	12072942	12072943	A	G	46	GENIC	homozygous	45684813
20	12073350	12073351	C	-	31	GENIC	homozygous	45430141
20	12073365	12073366	C	T	30	GENIC	homozygous	45684814
20	12073378	12073379	T	C	32	GENIC	homozygous	45430142
20	12073381	12073382	A	-	26	GENIC	homozygous	45684815
20	12073417	12073418	A	ACTGGCACT	21	GENIC	homozygous	45430143
20	12073990	12073991	A	T	24	GENIC	heterozygous	45430148
20	12074418	12074419	A	G	25	GENIC	heterozygous	45799219
20	12074484	12074485	G	A	38	GENIC	heterozygous	45430150
20	12074488	12074489	G	A	39	GENIC	heterozygous	45430151
20	12074489	12074490	A	-	20	GENIC	possibly homozygous	45684816
20	12075331	12075332	T	C	46	GENIC	homozygous	45430152
20	12075380	12075381	T	C	41	GENIC	homozygous	45430153
20	12075390	12075391	C	G	37	GENIC	homozygous	45430154