chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	10635035	10635036	T	C	46	GENIC	homozygous	111445105
3	10635767	10635768	T	G	71	GENIC	homozygous	111445107
3	10641844	10641845	G	A	45	GENIC	homozygous	111445127
3	10642184	10642185	T		43	GENIC	homozygous	130900545
3	10642186	10642194	AGCCCTAC		44	GENIC	homozygous	130900546
3	10649347	10649348	C	T	54	GENIC	homozygous	111874879
3	10656438	10656439	C	G	45	GENIC	homozygous	111445193
3	10666708	10666710	TT		51	GENIC	homozygous	127849106
3	10671049	10671053	AAAC		47	GENIC	homozygous	127849107
3	10677411	10677412	C	T	36	GENIC	homozygous	111874883
3	10680029	10680030	T	C	52	GENIC	homozygous	111445279
3	10684957	10684958	T	C	21	GENIC	homozygous	111874885
3	10685853	10685853		C	20	GENIC	homozygous	127849115
3	10686124	10686124		A	31	GENIC	homozygous	127849123
3	10688378	10688379	C	T	41	GENIC	homozygous	111445295
3	10689476	10689479	CCC		31	GENIC	possibly homozygous	127849124
3	10689845	10689846	A	T	48	GENIC	homozygous	111445299
3	10691207	10691207		G	4	GENIC	heterozygous	132287902
3	10691234	10691234		CAAAAACAAACAAAC	4	GENIC	heterozygous	127849126
3	10691923	10691924	A	G	27	GENIC	homozygous	111874887
3	10692095	10692096	T	A	43	GENIC	homozygous	111445303
3	10692109	10692110	A	G	42	GENIC	homozygous	111445305
3	10692355	10692356	C	T	18	GENIC	homozygous	111874889
3	10692892	10692893	C	T	28	GENIC	homozygous	111874897
3	10693569	10693570	C	T	44	GENIC	homozygous	111445309
3	10694042	10694049	AAAAAAA		49	GENIC	homozygous	127849129
3	10694234	10694235	G	A	48	GENIC	homozygous	111445311
3	10686113	10686113		TA	30	GENIC	homozygous	130277327