chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12071850	12071851	T	TA	30	GENIC	homozygous	45430122
20	12072129	12072130	G	A	19	GENIC	homozygous	45430125
20	12072140	12072141	A	G	19	GENIC	homozygous	45430126
20	12072605	12072606	A	G	25	GENIC	homozygous	45430137
20	12072708	12072709	C	A	27	GENIC	homozygous	45430138
20	12072847	12072848	T	C	34	GENIC	homozygous	45430139
20	12073141	12073142	G	T	32	GENIC	homozygous	45430140
20	12073350	12073351	C	-	22	GENIC	homozygous	45430141
20	12073365	12073366	C	T	17	GENIC	homozygous	45684814
20	12073378	12073379	T	C	21	GENIC	homozygous	45430142
20	12073381	12073382	A	-	23	GENIC	homozygous	45684815
20	12073417	12073418	A	ACTGGCACT	24	GENIC	homozygous	45430143
20	12073671	12073672	T	C	16	GENIC	homozygous	45430144
20	12073737	12073738	A	G	16	GENIC	possibly homozygous	45430145
20	12073756	12073757	G	A	14	GENIC	heterozygous	45430146
20	12073972	12073973	C	CTTT	4	GENIC	heterozygous	45900543
20	12075380	12075381	T	C	16	GENIC	homozygous	45430153
20	12074465	12074466	G	GAAAAAA	5	GENIC	homozygous	45842611