chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12071850	12071851	T	TA	13	GENIC	homozygous	45430122
20	12072354	12072355	C	T	23	GENIC	homozygous	45430131
20	12072589	12072590	C	G	25	GENIC	homozygous	45684809
20	12072655	12072656	G	A	23	GENIC	homozygous	45684810
20	12072708	12072709	C	A	28	GENIC	homozygous	45430138
20	12072847	12072848	T	C	23	GENIC	homozygous	45430139
20	12072900	12072901	C	T	21	GENIC	homozygous	45684811
20	12072929	12072930	C	T	22	GENIC	homozygous	45684812
20	12072942	12072943	A	G	23	GENIC	homozygous	45684813
20	12073350	12073351	C	-	16	GENIC	homozygous	45430141
20	12073365	12073366	C	T	18	GENIC	homozygous	45684814
20	12073378	12073379	T	C	14	GENIC	homozygous	45430142
20	12073381	12073382	A	-	12	GENIC	homozygous	45684815
20	12073417	12073418	A	ACTGGCACT	13	GENIC	homozygous	45430143
20	12073990	12073991	A	T	29	GENIC	heterozygous	45430148
20	12074484	12074485	G	A	29	GENIC	heterozygous	45430150
20	12074488	12074489	G	A	27	GENIC	heterozygous	45430151
20	12074489	12074490	A	-	14	GENIC	heterozygous	45684816
20	12075331	12075332	T	C	30	GENIC	homozygous	45430152
20	12075380	12075381	T	C	27	GENIC	homozygous	45430153
20	12075390	12075391	C	G	29	GENIC	homozygous	45430154