chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	90502205	90502206	G	C	32	GENIC	homozygous	61462328
1	90503113	90503114	C	-	10	GENIC	homozygous	62569689
1	90503115	90503140	CTCTCTCTCTCTCTCTCTCTCTCTC	-------------------------	12	GENIC	homozygous	62534948
1	90504528	90504529	T	C	22	GENIC	homozygous	61462332
1	90504968	90504969	C	CTTTT	7	GENIC	heterozygous	62140640
1	90504969	90504970	T	-	7	GENIC	heterozygous	62311333
1	90505045	90505046	A	G	21	GENIC	possibly homozygous	61462334
1	90505106	90505107	A	G	16	GENIC	homozygous	61462335
1	90507347	90507348	T	C	28	GENIC	homozygous	61462341
1	90507868	90507869	C	T	23	GENIC	homozygous	61462343
1	90508250	90508251	T	C	16	GENIC	homozygous	61462345
1	90511931	90511932	C	-	15	GENIC	homozygous	61462350
1	90512343	90512344	A	G	24	GENIC	heterozygous	62264060
1	90513060	90513061	T	C	42	GENIC	homozygous	61462357
1	90513845	90513846	A	G	30	GENIC	homozygous	61462361
1	90514473	90514474	C	A	32	GENIC	homozygous	61462363
1	90516248	90516249	G	A	34	GENIC	homozygous	61462365
1	90503588	90503589	G	A	25	GENIC	homozygous	61888169
1	90504259	90504260	C	T	11	GENIC	homozygous	61888170
1	90509102	90509103	T	TAAA	21	GENIC	homozygous	61888171
1	90509821	90509822	G	GTGAATGAATGAATGAATGAATGAA	8	GENIC	homozygous	62650118