chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	110457807	110457808	G	A	69	GENIC	homozygous	138181217
7	110458060	110458061	G	A	59	GENIC	homozygous	138181218
7	110458914	110458915	C	T	62	GENIC	homozygous	138181219
7	110459181	110459181		G	8	GENIC	homozygous	137974054
7	110459281	110459282	A	G	36	GENIC	homozygous	138181220
7	110459518	110459519	C		54	GENIC	homozygous	137974055
7	110461756	110461757	T	C	63	GENIC	homozygous	138181221
7	110461914	110461915	G	T	91	GENIC	possibly homozygous	138181222
7	110462697	110462698	A	G	74	GENIC	homozygous	138181223
7	110463549	110463550	C	A	66	GENIC	possibly homozygous	138181224
7	110465274	110465275	T	C	85	GENIC	possibly homozygous	138181225
7	110465485	110465486	A	T	70	GENIC	homozygous	138181226
7	110465860	110465861	T	C	72	GENIC	homozygous	138181227
7	110466958	110466962	GGGT		57	GENIC	possibly homozygous	137974056
7	110467240	110467241	A	G	69	GENIC	homozygous	138181228
7	110467276	110467280	CTTT		48	GENIC	homozygous	137974057
7	110467761	110467762	T		67	GENIC	homozygous	137974058
7	110467857	110467858	A	C	74	GENIC	homozygous	138181229
7	110467919	110467920	A	C	66	GENIC	homozygous	138181230
7	110468373	110468374	A	G	85	GENIC	homozygous	138181231
7	110468422	110468423	A	G	78	GENIC	homozygous	138181232
7	110468978	110468979	C	T	60	GENIC	homozygous	138181233
7	110469228	110469229	T	C	65	GENIC	homozygous	138181234
7	110469420	110469421	C	T	81	GENIC	homozygous	138181235
7	110469548	110469549	T	C	69	GENIC	homozygous	138181236
7	110469704	110469705	C	T	72	GENIC	homozygous	138181237
7	110466961	110466962	T		57	GENIC	possibly homozygous	403222297
7	110466961	110466962	T	G	57	GENIC	heterozygous	154485220
7	110467313	110467314	T	A	70	GENIC	homozygous	403222298
7	110467313	110467314	T		70	GENIC	heterozygous	403222299