chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	126887270	126887271	C	T	24	GENIC	homozygous	113302598
4	126887411	126887412	A	T	23	GENIC	homozygous	113302599
4	126887674	126887675	G	A	28	GENIC	possibly homozygous	119535472
4	126887845	126887846	T	C	13	GENIC	homozygous	113302600
4	126887881	126887882	G	A	13	GENIC	homozygous	113302601
4	126888179	126888180	G	T	23	GENIC	homozygous	113302602
4	126888971	126888972	G	C	27	GENIC	homozygous	113302608
4	126888975	126888976	G	A	28	GENIC	homozygous	113302609
4	126888986	126888987	T	C	28	GENIC	homozygous	113302610
4	126889256	126889257	C	T	26	GENIC	homozygous	113302611
4	126889541	126889542	C	A	27	GENIC	homozygous	113302612
4	126890219	126890220	T	C	16	GENIC	homozygous	113302613
4	126890357	126890358	T	G	39	GENIC	homozygous	113302616
4	126891195	126891196	G	T	33	GENIC	homozygous	113302617
4	126891402	126891403	A	G	31	GENIC	possibly homozygous	119409574
4	126892077	126892078	T	C	22	GENIC	homozygous	113302620
4	126892845	126892846	C	T	33	GENIC	possibly homozygous	119409575
4	126892924	126892925	C	T	31	GENIC	possibly homozygous	119409576
4	126893107	126893108	A	G	31	GENIC	homozygous	113302622
4	126893825	126893826	T	C	14	GENIC	homozygous	113302623
4	126895010	126895011	A	G	26	GENIC	homozygous	119409577
4	126895146	126895147	T	G	23	GENIC	homozygous	119409578
4	126896108	126896109	T	C	24	GENIC	possibly homozygous	119409579
4	126897005	126897006	A	C	25	GENIC	possibly homozygous	119409580
4	126897064	126897065	C	T	32	GENIC	possibly homozygous	119409581
4	126897166	126897167	T	C	17	GENIC	homozygous	119409582
4	126897491	126897492	T	C	18	GENIC	homozygous	113302624
4	126898592	126898593	G	A	29	GENIC	homozygous	119409583