chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	76736464	76736464		TATG	39	GENIC	homozygous	145393783
3	76744804	76744805	G	A	45	GENIC	homozygous	145415297
3	76748669	76748670	T		45	GENIC	homozygous	145393784
3	76748670	76748671	T	A	45	GENIC	homozygous	145415298
3	76749916	76749917	C	T	48	GENIC	homozygous	145415299
3	76751039	76751040	G	C	46	GENIC	homozygous	136754910
3	76751603	76751604	G	A	34	GENIC	homozygous	136754912
3	76752191	76752192	T		35	GENIC	homozygous	136574118
3	76752325	76752326	T	G	20	GENIC	homozygous	145415300
3	76752754	76752755	A	C	37	GENIC	homozygous	136754913
3	76753248	76753249	T	C	40	GENIC	homozygous	136754914
3	76753680	76753681	C	T	44	GENIC	homozygous	145415301
3	76753945	76753946	T	C	35	GENIC	homozygous	145415302
3	76754068	76754069	A	C	42	GENIC	homozygous	145415303
3	76754581	76754582	T	C	41	GENIC	homozygous	136754916
3	76754967	76754968	A	G	31	GENIC	homozygous	145415304
3	76755349	76755350	C	G	33	GENIC	homozygous	145415305
3	76755474	76755475	A	G	30	GENIC	possibly homozygous	145415306
3	76755544	76755545	G	T	44	GENIC	homozygous	145415307
3	76755817	76755818	G	A	38	GENIC	homozygous	136754918
3	76756384	76756385	A	T	45	GENIC	homozygous	145415308
3	76757408	76757409	G	A	36	GENIC	homozygous	145415309
3	76757476	76757478	AG		27	GENIC	possibly homozygous	145393785
3	76757482	76757483	T	G	32	GENIC	homozygous	136754921
3	76758922	76758924	TG		33	GENIC	homozygous	145393786
3	76758939	76758940	T	G	33	GENIC	homozygous	145415310
3	76758957	76758960	TTC		37	GENIC	homozygous	136574123
3	76759046	76759047	G	A	39	GENIC	homozygous	136754922
3	76760106	76760107	C	T	53	GENIC	homozygous	145415311
3	76760614	76760614		T	33	GENIC	possibly homozygous	148682318
3	76761550	76761551	G	A	39	GENIC	homozygous	136754924
3	76761580	76761581	C	T	42	GENIC	homozygous	136754925
3	76761704	76761705	C	T	44	GENIC	homozygous	136754926
3	76762296	76762297	C	T	48	GENIC	homozygous	136754929
3	76762888	76762889	T	C	45	GENIC	homozygous	136754930