chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	141561951	141561952	C	T	35	GENIC	homozygous	108261204
1	141561967	141561968	C	T	32	GENIC	possibly homozygous	109327648
1	141562269	141562270	T	A	19	GENIC	homozygous	108261210
1	141562588	141562589	A	G	16	GENIC	homozygous	108261227
1	141563005	141563006	G	A	7	GENIC	homozygous	109327650
1	141563248	141563249	C	T	27	GENIC	possibly homozygous	109049571
1	141563661	141563662	A	G	38	GENIC	possibly homozygous	109049572
1	141563867	141563868	A	T	31	GENIC	homozygous	108261237
1	141563923	141563924	A	G	26	GENIC	homozygous	108261239
1	141565166	141565167	T	G	43	GENIC	homozygous	108261245
1	141565380	141565381	G	T	29	GENIC	homozygous	109327651
1	141565891	141565892	C	G	23	GENIC	homozygous	109327660
1	141566613	141566614	T	C	33	GENIC	homozygous	108261268
1	141567083	141567084	C	T	28	GENIC	homozygous	109049576
1	141567122	141567123	T	C	28	GENIC	homozygous	109049577
1	141569911	141569912	A	T	12	GENIC	homozygous	108261282
1	141574708	141574709	G	A	8	GENIC	homozygous	109327661
1	141575176	141575177	G	C	25	GENIC	possibly homozygous	109327662
1	141576900	141576901	G	A	29	GENIC	homozygous	109327663
1	141577958	141577959	G	A	26	GENIC	homozygous	109327664
1	141579439	141579440	G	A	32	GENIC	homozygous	109327665
1	141585104	141585105	A	G	16	GENIC	homozygous	108261310
1	141590113	141590114	G	A	32	GENIC	homozygous	109327667
1	141597348	141597349	T	C	36	GENIC	homozygous	108261354
1	141598808	141598809	G	A	25	GENIC	homozygous	108261364
1	141598857	141598858	T	C	22	GENIC	homozygous	108261366
1	141599088	141599089	C	T	22	GENIC	homozygous	109327670
1	141600146	141600147	G	A	13	GENIC	possibly homozygous	109327671
1	141601232	141601233	G	A	24	GENIC	homozygous	109327672
1	141603149	141603150	A	G	39	GENIC	possibly homozygous	108936987
1	141603333	141603334	A	G	39	GENIC	possibly homozygous	108261372
1	141603989	141603990	A	G	30	GENIC	homozygous	108261376