chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	3433947	3433948	G	GCTCT	30	GENIC	homozygous	62117591
1	3433951	3433954	CCC	---	33	GENIC	homozygous	62117592
1	3433955	3433956	C	CGTTTTG	32	GENIC	homozygous	62117593
1	3435087	3435105	GTGTGTGTGTGTGTGTGT	------------------	15	GENIC	homozygous	62659440
1	3436860	3436861	T	C	23	GENIC	homozygous	60595916
1	3437305	3437306	T	-	15	GENIC	homozygous	60595918
1	3437820	3437821	G	A	13	GENIC	homozygous	62659441
1	3438673	3438674	C	T	32	GENIC	homozygous	60595924
1	3438721	3438722	A	-	30	GENIC	homozygous	60595926
1	3438917	3438918	T	C	23	GENIC	homozygous	62659442
1	3439325	3439326	C	T	18	GENIC	homozygous	60595930
1	3439635	3439637	TT	--	18	GENIC	possibly homozygous	62659443
1	3441497	3441498	G	A	20	GENIC	homozygous	61660964
1	3442620	3442621	G	A	26	GENIC	homozygous	60595946
1	3442621	3442622	A	C	27	GENIC	homozygous	60595948
1	3444518	3444519	T	TTTG	27	GENIC	homozygous	60595966
1	3446131	3446132	G	A	20	GENIC	homozygous	62659444
1	3446913	3446914	C	T	20	GENIC	homozygous	62659445
1	3449589	3449591	AC	--	25	GENIC	homozygous	61660967
1	3451178	3451179	G	A	25	GENIC	homozygous	62659446
1	3452080	3452081	A	G	17	GENIC	homozygous	60596004
1	3453126	3453127	T	C	30	GENIC	homozygous	62659447
1	3453302	3453303	G	C	32	GENIC	homozygous	61660969
1	3454739	3454740	A	-	8	GENIC	homozygous	62445491
1	3455486	3455488	AA	--	7	GENIC	homozygous	62466781
1	3459782	3459783	A	AT	29	GENIC	possibly homozygous	62659448
1	3459979	3459980	G	A	18	GENIC	homozygous	60596074
1	3461249	3461250	C	T	22	GENIC	homozygous	60596082
1	3461848	3461849	A	G	32	GENIC	homozygous	60596084
1	3462781	3462782	T	G	16	GENIC	homozygous	60596106