chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	141393314	141393315	G	A	45	GENIC	homozygous	108260621
1	141397497	141397498	T	C	44	GENIC	homozygous	108260623
1	141398554	141398555	A	C	28	GENIC	possibly homozygous	108260625
1	141399178	141399179	T	C	45	GENIC	homozygous	108260631
1	141402640	141402641	C	T	37	GENIC	homozygous	108260633
1	141404079	141404080	C	T	49	GENIC	homozygous	108260635
1	141409109	141409110	C	T	45	GENIC	homozygous	108260637
1	141411361	141411362	T	C	50	GENIC	homozygous	108260639
1	141417372	141417373	G	C	43	GENIC	homozygous	108260641
1	141418043	141418044	C	T	40	GENIC	homozygous	108260643
1	141419202	141419203	T	G	52	GENIC	homozygous	108260645
1	141419575	141419576	C	T	43	GENIC	homozygous	108260647
1	141422132	141422133	G	A	42	GENIC	homozygous	108260649
1	141398638	141398638		GG	39	GENIC	possibly homozygous	127438906
1	141403459	141403460	G		49	GENIC	homozygous	127438907
1	141427913	141427914	A	T	43	GENIC	homozygous	108260653
1	141430190	141430191	G	A	37	GENIC	homozygous	108260655
1	141430505	141430506	C	T	54	GENIC	possibly homozygous	108260657
1	141430652	141430653	C	T	47	GENIC	homozygous	108260659
1	141431634	141431635	T	C	53	GENIC	homozygous	108260661
1	141431976	141431977	T	C	40	GENIC	homozygous	108260663
1	141433311	141433330	CTTCATATGAGGCCAGGCC		50	GENIC	homozygous	127438910