chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	128028359	128028360	T	C	30	GENIC	homozygous	52884672
8	128028481	128028482	C	CTTTTA	10	GENIC	homozygous	52884673
8	128029653	128029654	C	CTT	19	GENIC	homozygous	52884674
8	128029661	128029662	T	TTTG	21	GENIC	homozygous	52884675
8	128029662	128029663	G	GTT	10	GENIC	heterozygous	52884676
8	128029662	128029663	G	GGTT	10	GENIC	possibly homozygous	52884677
8	128030090	128030091	T	C	21	GENIC	homozygous	52884678
8	128030446	128030447	T	C	27	GENIC	homozygous	52884679
8	128031132	128031133	G	A	29	GENIC	homozygous	52884680
8	128031353	128031354	C	T	40	GENIC	homozygous	52884681
8	128031364	128031365	C	T	40	GENIC	homozygous	52884682
8	128032203	128032204	G	A	37	GENIC	homozygous	52884683
8	128032444	128032445	T	C	28	GENIC	homozygous	52884684
8	128032728	128032729	A	ACAC	26	GENIC	heterozygous	52884685
8	128033460	128033461	A	G	29	GENIC	homozygous	52884686
8	128033467	128033468	T	A	29	GENIC	homozygous	52884687
8	128034345	128034346	A	AT	16	GENIC	possibly homozygous	52884688
8	128034346	128034347	A	T	18	GENIC	homozygous	53064453
8	128034693	128034695	CT	--	14	GENIC	homozygous	52884689
8	128034695	128034701	CTTACC	------	12	GENIC	heterozygous	52884690
8	128034695	128034696	C	-	12	GENIC	heterozygous	52884691
8	128034696	128034699	TTA	---	15	GENIC	homozygous	52884692
8	128034697	128034699	TA	--	15	GENIC	homozygous	52884693
8	128035400	128035401	A	AC	18	GENIC	homozygous	52884694
8	128035410	128035411	C	CA	23	GENIC	homozygous	52884695
8	128035473	128035474	G	A	43	GENIC	homozygous	52884696
8	128035655	128035656	T	TGG	29	GENIC	homozygous	52884697
8	128036029	128036030	T	-	13	GENIC	heterozygous	53171959