chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	13673374	13673375	G	C	13	GENIC	heterozygous	45434411
20	13678096	13678097	G	A	28	GENIC	heterozygous	45434448
20	13678143	13678144	A	G	32	GENIC	heterozygous	45687904
20	13678153	13678154	A	G	31	GENIC	heterozygous	45687905
20	13678190	13678191	G	GA	31	GENIC	heterozygous	45687906
20	13678197	13678198	A	G	34	GENIC	heterozygous	45687907
20	13678203	13678204	G	GAGA	33	GENIC	heterozygous	45687908
20	13678207	13678208	C	G	33	GENIC	heterozygous	45843157
20	13678210	13678211	T	C	33	GENIC	heterozygous	45687909
20	13678214	13678215	C	T	31	GENIC	heterozygous	45687910
20	13678217	13678218	A	G	31	GENIC	heterozygous	45687911
20	13678402	13678403	C	T	8	GENIC	heterozygous	45687912
20	13678445	13678446	G	GTCCA	16	GENIC	homozygous	45434450
20	13679159	13679160	G	GT	4	GENIC	heterozygous	45859314
20	13679160	13679161	T	-	4	GENIC	heterozygous	45863999
20	13679187	13679188	C	T	12	GENIC	heterozygous	45687913
20	13680774	13680775	A	AATCCTAT	24	GENIC	homozygous	45434468
20	13681661	13681662	G	GT	14	GENIC	homozygous	45434474
20	13685993	13685994	T	TTG	11	GENIC	heterozygous	45843158
20	13686000	13686002	TG	--	11	GENIC	heterozygous	45687919
20	13687718	13687719	C	T	22	GENIC	heterozygous	45687921
20	13689924	13689925	G	GA	15	GENIC	possibly homozygous	45434514
20	13689927	13689928	C	CAA	8	GENIC	heterozygous	45894803
20	13680835	13680836	A	T	24	GENIC	homozygous	45623022
20	13685998	13686002	TGTG	----	11	GENIC	heterozygous	45738932