chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	212727237	212727241	TTTG	----	8	GENIC	homozygous	61076601
1	212728962	212728963	G	GA	6	GENIC	homozygous	61076602
1	212729890	212729891	A	G	21	GENIC	homozygous	61076604
1	212731849	212731850	A	G	18	GENIC	possibly homozygous	61076606
1	212732133	212732134	T	A	2	GENIC	homozygous	61076607
1	212732283	212732284	T	C	8	GENIC	possibly homozygous	61076608
1	212732898	212732899	A	G	21	GENIC	possibly homozygous	61076609
1	212732908	212732909	G	A	17	GENIC	possibly homozygous	61076610
1	212733279	212733280	A	G	19	GENIC	homozygous	61076611
1	212733415	212733416	T	C	22	GENIC	possibly homozygous	61076612
1	212733798	212733799	A	AAAAC	2	GENIC	heterozygous	62302258
1	212734086	212734087	C	G	26	GENIC	homozygous	61076617
1	212734571	212734572	C	T	20	GENIC	possibly homozygous	61076618
1	212734635	212734636	T	C	17	GENIC	homozygous	61076619
1	212735014	212735015	T	TC	27	GENIC	possibly homozygous	61076620
1	212735154	212735155	A	G	34	GENIC	homozygous	61076621
1	212736346	212736376	GCTGTGTCCCTTGTGTAGACAGGCATGCTG	------------------------------	12	GENIC	possibly homozygous	62098804
1	212736629	212736630	C	T	15	GENIC	homozygous	61076624
1	212736674	212736675	A	T	21	GENIC	possibly homozygous	61076625
1	212736689	212736690	G	A	20	GENIC	possibly homozygous	61076626
1	212737698	212737699	T	C	24	GENIC	homozygous	61076627
1	212738397	212738398	T	G	25	GENIC	possibly homozygous	61076628
1	212738749	212738750	G	A	15	GENIC	homozygous	61076629