chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	100990278	100990279	C	T	42	GENIC	homozygous	114437747
13	100991019	100991020	A	G	38	GENIC	homozygous	114437749
13	100991268	100991269	C	A	12	GENIC	homozygous	114437751
13	100992401	100992402	A	G	48	GENIC	heterozygous	118467476
13	100992402	100992403	T	C	59	GENIC	heterozygous	118467477
13	100993926	100993927	C	A	80	GENIC	heterozygous	118467478
13	100994546	100994547	A	G	27	GENIC	possibly homozygous	118467479
13	100994575	100994576	A	C	12	GENIC	homozygous	118467480
13	100994693	100994694	A	T	9	GENIC	possibly homozygous	118467481
13	100995451	100995452	C	T	125	GENIC	heterozygous	118467482
13	100995497	100995498	G	A	108	GENIC	heterozygous	118467483
13	100995531	100995532	G	C	72	GENIC	heterozygous	118467484
13	100995759	100995760	C	T	91	GENIC	heterozygous	118467485
13	100995763	100995764	A	G	82	GENIC	heterozygous	118467486
13	101024473	101024474	G	A	56	GENIC	homozygous	114437759
13	101031462	101031463	A	C	25	GENIC	homozygous	118467487
13	101031631	101031632	G	C	37	GENIC	homozygous	114437761
13	101031634	101031635	A	T	38	GENIC	homozygous	114437763
13	101031924	101031925	G	A	61	GENIC	homozygous	114437765