chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	100787522	100787523	T	C	14	GENIC	homozygous	61483700
1	100787598	100787599	G	-	10	GENIC	homozygous	61731891
1	100787600	100787601	G	A	11	GENIC	heterozygous	62146849
1	100787893	100787894	A	G	17	GENIC	homozygous	61483701
1	100787941	100787942	C	T	20	GENIC	homozygous	61731893
1	100788109	100788110	C	T	12	GENIC	homozygous	61483702
1	100788274	100788275	C	T	15	GENIC	homozygous	61731895
1	100788323	100788324	G	A	17	GENIC	homozygous	61731897
1	100788398	100788399	C	CCT	13	GENIC	homozygous	61483705
1	100788402	100788403	T	C	13	GENIC	homozygous	61483706
1	100788504	100788505	A	AC	9	GENIC	homozygous	61731899
1	100790620	100790621	C	T	25	GENIC	homozygous	61731901
1	100791154	100791155	C	A	12	GENIC	homozygous	61731903
1	100791381	100791393	GTGTGTGTGTGT	------------	10	GENIC	heterozygous	62146851
1	100791383	100791393	GTGTGTGTGT	----------	10	GENIC	heterozygous	62146853