chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	101055866	101055867	G	A	23	GENIC	heterozygous	62065458
1	101056512	101056513	G	T	12	GENIC	homozygous	62065459
1	101056685	101056686	C	T	11	GENIC	heterozygous	62065460
1	101057783	101057784	C	CA	14	GENIC	homozygous	62065461
1	101057964	101057965	A	AC	22	GENIC	heterozygous	60779712
1	101058078	101058079	A	-	14	GENIC	possibly homozygous	60779715
1	101061487	101061488	T	C	13	GENIC	possibly homozygous	62065465
1	101061852	101061853	A	G	16	GENIC	possibly homozygous	62065466
1	101062535	101062536	C	G	5	GENIC	heterozygous	61484011
1	101062870	101062871	C	T	11	GENIC	heterozygous	62065467
1	101063776	101063777	A	AC	8	GENIC	heterozygous	61484012
1	101063982	101063983	T	C	15	GENIC	homozygous	61484013
1	101065609	101065610	T	C	5	GENIC	homozygous	62065468
1	101066429	101066430	C	T	19	GENIC	homozygous	62065469
1	101066766	101066767	T	TC	9	GENIC	possibly homozygous	62065470
1	101066783	101066784	T	C	10	GENIC	possibly homozygous	62065471
1	101067320	101067321	C	A	17	GENIC	heterozygous	62065472
1	101067457	101067458	A	-	8	GENIC	heterozygous	61484022
1	101067728	101067729	T	C	8	GENIC	homozygous	62065473
1	101068276	101068277	T	TC	10	GENIC	possibly homozygous	61484024
1	101068413	101068414	C	A	5	GENIC	homozygous	62065474
1	101068489	101068490	C	CT	15	GENIC	homozygous	62065475