chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	82187585	82187597	GTGTGTGTGTGC	------------	13	GENIC	heterozygous	61448666
1	82187670	82187671	A	-	11	GENIC	heterozygous	61448667
1	82188310	82188311	T	C	11	GENIC	heterozygous	61448668
1	82192860	82192861	T	TTGTG	11	GENIC	heterozygous	61448671
1	82194883	82194884	C	G	20	GENIC	heterozygous	61448673
1	82194908	82194909	A	G	15	GENIC	heterozygous	61448674
1	82194932	82194933	G	C	12	GENIC	heterozygous	61448675
1	82194953	82194954	A	T	11	GENIC	heterozygous	61448676
1	82194983	82194984	A	G	9	GENIC	heterozygous	61448677
1	82194996	82194997	G	A	11	GENIC	heterozygous	61448678
1	82195117	82195118	A	T	12	GENIC	heterozygous	62758056
1	82195646	82195647	A	G	11	GENIC	heterozygous	61448679
1	82195826	82195827	T	C	16	GENIC	heterozygous	61448680
1	82196117	82196118	T	C	21	GENIC	heterozygous	61448681
1	82196452	82196453	C	T	10	GENIC	heterozygous	61448683
1	82196745	82196746	T	A	23	GENIC	heterozygous	61448684
1	82197194	82197195	A	AG	19	GENIC	heterozygous	61448685
1	82197262	82197263	A	G	13	GENIC	heterozygous	61448686
1	82198139	82198140	C	A	9	GENIC	heterozygous	61448688
1	82198389	82198390	A	G	14	GENIC	heterozygous	61448689
1	82198869	82198870	G	A	16	GENIC	heterozygous	61448690
1	82198882	82198883	C	A	14	GENIC	heterozygous	61448691
1	82198943	82198944	C	T	14	GENIC	heterozygous	61448692
1	82200605	82200606	T	C	16	GENIC	heterozygous	61448693
1	82200699	82200700	G	C	18	GENIC	heterozygous	61448694
1	82200788	82200789	A	C	12	GENIC	heterozygous	61448695
1	82200920	82200921	G	A	22	GENIC	heterozygous	61448696
1	82201219	82201220	C	T	22	GENIC	heterozygous	61448697
1	82201526	82201527	C	A	13	GENIC	heterozygous	61448698
1	82202113	82202114	G	T	20	GENIC	heterozygous	61448699
1	82202636	82202637	G	A	15	GENIC	heterozygous	61448700
1	82203823	82203824	T	A	17	GENIC	heterozygous	61448701
1	82204141	82204142	C	T	17	GENIC	heterozygous	61448702