chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	12974097	12974098	C	T	6	GENIC	homozygous	126680770
8	12974824	12974825	T		34	GENIC	homozygous	131041321
8	12977554	12977555	G	A	25	GENIC	homozygous	117090122
8	12975822	12975823	G	C	32	GENIC	homozygous	117090119
8	12976138	12976139	A	G	21	GENIC	homozygous	117090120
8	12976185	12976186	C	T	26	GENIC	homozygous	117090121
8	12977866	12977867	C	T	33	GENIC	homozygous	117090123
8	12978293	12978294	A	G	20	GENIC	homozygous	117090124
8	12979622	12979623	A	G	32	GENIC	homozygous	117090125
8	12983667	12983668	A		20	GENIC	homozygous	131041322
8	12983943	12983943		C	21	GENIC	homozygous	131041323
8	12984333	12984333		A	31	GENIC	homozygous	131041324
8	12987329	12987339	GGTGAGGTGA		8	GENIC	homozygous	131041325
8	12987464	12987465	C	A	6	GENIC	homozygous	117090135
8	12979998	12979999	C	T	28	GENIC	homozygous	117090126
8	12980687	12980688	G	A	20	GENIC	homozygous	117090127
8	12982267	12982268	C	T	33	GENIC	homozygous	117090129
8	12984172	12984173	G	A	37	GENIC	homozygous	117090130
8	12987451	12987452	G	A	7	GENIC	homozygous	117090133
8	12987454	12987455	A	C	7	GENIC	homozygous	117090134
8	12989281	12989282	C		28	GENIC	homozygous	131041326
8	12989902	12989906	ATGT		26	GENIC	homozygous	131041327
8	12990185	12990186	T		25	GENIC	homozygous	131041328
8	12991996	12991997	T		37	GENIC	homozygous	131041329
8	12992442	12992443	C	T	39	GENIC	homozygous	117090142
8	12992860	12992861	G	T	28	GENIC	homozygous	117090143
8	12993163	12993164	A	G	12	GENIC	homozygous	117090144
8	12993181	12993182	G	A	12	GENIC	homozygous	117090145