chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	128028359	128028360	T	C	28	GENIC	homozygous	52884672
8	128028481	128028482	C	CTTTTA	3	GENIC	heterozygous	52884673
8	128030090	128030091	T	C	10	GENIC	homozygous	52884678
8	128030446	128030447	T	C	21	GENIC	homozygous	52884679
8	128031132	128031133	G	A	25	GENIC	possibly homozygous	52884680
8	128031353	128031354	C	T	13	GENIC	heterozygous	52884681
8	128031364	128031365	C	T	19	GENIC	homozygous	52884682
8	128032203	128032204	G	A	21	GENIC	possibly homozygous	52884683
8	128032444	128032445	T	C	22	GENIC	homozygous	52884684
8	128033460	128033461	A	G	14	GENIC	possibly homozygous	52884686
8	128033467	128033468	T	A	13	GENIC	heterozygous	52884687
8	128034345	128034346	A	AT	4	GENIC	homozygous	52884688
8	128034346	128034347	A	T	4	GENIC	homozygous	53064453
8	128035410	128035411	C	CA	5	GENIC	homozygous	52884695
8	128035473	128035474	G	A	29	GENIC	homozygous	52884696
8	128035655	128035656	T	TGG	4	GENIC	heterozygous	52884697