chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	10635035	10635036	T	C	25	GENIC	homozygous	111445105
3	10635767	10635768	T	G	14	GENIC	homozygous	111445107
3	10639095	10639107	TCTCCACGCCGT		15	GENIC	homozygous	132038480
3	10641844	10641845	G	A	26	GENIC	homozygous	111445127
3	10656438	10656439	C	G	24	GENIC	homozygous	111445193
3	10666708	10666710	TT		18	GENIC	homozygous	127849106
3	10668536	10668537	C	T	15	GENIC	homozygous	112065600
3	10642130	10642131	C	T	24	GENIC	homozygous	112065592
3	10644295	10644296	C	T	23	GENIC	homozygous	112065594
3	10646241	10646242	C	A	15	GENIC	homozygous	112065596
3	10657037	10657038	G	A	15	GENIC	homozygous	112065598
3	10670333	10670334	G	A	19	GENIC	homozygous	112065602
3	10670858	10670859	C	T	23	GENIC	homozygous	112065604
3	10671049	10671053	AAAC		16	GENIC	homozygous	127849107
3	10680029	10680030	T	C	22	GENIC	homozygous	111445279
3	10685616	10685617	C		7	GENIC	homozygous	130277326
3	10685621	10685622	C		7	GENIC	homozygous	132038481
3	10685853	10685853		C	6	GENIC	homozygous	127849115
3	10686113	10686113		TA	13	GENIC	homozygous	130277327
3	10686124	10686124		A	13	GENIC	homozygous	127849123
3	10688378	10688379	C	T	26	GENIC	homozygous	111445295
3	10689476	10689479	CCC		14	GENIC	homozygous	127849124
3	10689845	10689846	A	T	22	GENIC	homozygous	111445299
3	10691240	10691241	A	C	7	GENIC	homozygous	132045895
3	10691254	10691255	C		7	GENIC	homozygous	132038482
3	10691261	10691262	A	C	12	GENIC	homozygous	132045896
3	10691923	10691924	A	G	13	GENIC	homozygous	111874887
3	10692095	10692096	T	A	27	GENIC	homozygous	111445303
3	10692109	10692110	A	G	29	GENIC	homozygous	111445305
3	10693569	10693570	C	T	14	GENIC	homozygous	111445309
3	10694042	10694049	AAAAAAA		13	GENIC	homozygous	127849129
3	10694234	10694235	G	A	15	GENIC	homozygous	111445311