chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	1612777	1612778	C	T	8	GENIC	possibly homozygous	63321262
20	1613362	1613363	T	C	4	GENIC	homozygous	63321263
20	1613935	1613936	A	G	10	GENIC	homozygous	63321264
20	1615400	1615401	G	A	10	GENIC	homozygous	63321266
20	1615639	1615640	C	T	15	GENIC	homozygous	63321267
20	1616159	1616160	C	T	13	GENIC	homozygous	63321268
20	1616303	1616304	G	A	12	GENIC	homozygous	63321269
20	1616483	1616484	A	G	10	GENIC	homozygous	63321270
20	1616870	1616871	C	T	17	GENIC	homozygous	63321271
20	1617109	1617110	C	T	17	GENIC	homozygous	63321272
20	1617194	1617195	G	C	12	GENIC	homozygous	63321273
20	1617231	1617232	C	T	10	GENIC	homozygous	63321274
20	1617281	1617282	T	A	11	GENIC	homozygous	63321275
20	1617407	1617408	C	T	16	GENIC	homozygous	63321276
20	1617907	1617908	C	T	13	GENIC	homozygous	63321277