chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5056906	5056907	C	T	11	GENIC	homozygous	125176843
20	5056920	5056921	G	A	8	GENIC	homozygous	125176844
20	5056949	5056950	T	C	10	GENIC	homozygous	125176845
20	5056955	5056956	G	A	15	GENIC	homozygous	125176846
20	5057309	5057310	G	A	32	GENIC	homozygous	125221570
20	5057337	5057338	C	T	17	GENIC	homozygous	125176847
20	5057417	5057418	A	G	12	GENIC	homozygous	125176848
20	5057601	5057602	A	C	32	GENIC	homozygous	125176849
20	5057831	5057832	C	T	23	GENIC	homozygous	125221571
20	5058172	5058173	C	T	22	GENIC	homozygous	125221572
20	5058249	5058250	G	C	23	GENIC	homozygous	125176851
20	5058624	5058625	C	T	30	GENIC	homozygous	125221573
20	5058686	5058687	G	A	24	GENIC	homozygous	125221574
20	5058915	5058916	C	G	12	GENIC	homozygous	125176852
20	5059477	5059478	T	C	21	GENIC	homozygous	125176853
20	5059590	5059591	T	C	19	GENIC	homozygous	125221575
20	5059617	5059618	C	T	22	GENIC	homozygous	125176854
20	5059694	5059695	A	G	19	GENIC	homozygous	125176855
20	5060361	5060362	G	A	17	GENIC	homozygous	125221576