chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	103778966	103778967	G		51	GENIC	homozygous	128623608
8	103779373	103779374	T	A	45	GENIC	homozygous	116618921
8	103780270	103780271	T	C	27	GENIC	homozygous	116618933
8	103792107	103792108	T	G	14	GENIC	homozygous	116618947
8	103846110	103846110		AT	35	GENIC	heterozygous	128623633
8	103846111	103846113	CT		35	GENIC	heterozygous	128623634
8	103792110	103792110		A	14	GENIC	homozygous	129950657
8	103827996	103827996		TGGT	40	GENIC	homozygous	131052711
8	103835413	103835414	C	G	25	GENIC	homozygous	116984562
8	103835418	103835419	A	G	22	GENIC	homozygous	116984563
8	103846100	103846101	G	C	32	GENIC	heterozygous	131061067
8	103846104	103846105	G	A	32	GENIC	heterozygous	128665422
8	103846105	103846106	T	C	32	GENIC	heterozygous	128665423
8	103847285	103847286	A	G	20	GENIC	homozygous	116984564
8	103848919	103848920	G	A	45	GENIC	heterozygous	123031882
8	103849171	103849172	G	A	40	GENIC	heterozygous	130772099
8	103881255	103881256	A	C	39	GENIC	homozygous	116619156
8	103872059	103872059		G	9	GENIC	homozygous	132668839
8	103849140	103849141	C	A	43	GENIC	heterozygous	132673601