chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105618960	105618961	A	G	30	GENIC	homozygous	116837329
10	105620069	105620070	A	G	18	GENIC	homozygous	116837331
10	105620227	105620228	T	A	23	GENIC	homozygous	116837333
10	105620276	105620277	A	C	25	GENIC	homozygous	116837335
10	105620284	105620285	C	T	26	GENIC	homozygous	116837337
10	105620452	105620453	G	A	32	GENIC	homozygous	118088394
10	105620528	105620529	A	G	29	GENIC	homozygous	116837339
10	105620935	105620936	C	T	30	GENIC	homozygous	118088395
10	105621079	105621080	A	G	32	GENIC	possibly homozygous	117031771
10	105621430	105621431	A	G	30	GENIC	possibly homozygous	116837341
10	105621556	105621557	G	A	35	GENIC	homozygous	116837343
10	105621779	105621780	T	G	34	GENIC	homozygous	116837345
10	105621781	105621782	C	G	33	GENIC	homozygous	116837347
10	105622175	105622176	A	G	28	GENIC	homozygous	116837351
10	105622205	105622206	T	C	29	GENIC	possibly homozygous	116837353
10	105622209	105622210	A	C	29	GENIC	possibly homozygous	116837355
10	105622320	105622321	T	C	39	GENIC	homozygous	117031775
10	105622337	105622338	A	G	38	GENIC	homozygous	116837357
10	105622412	105622413	A	T	42	GENIC	homozygous	116837359
10	105622421	105622422	G	T	43	GENIC	homozygous	116837361
10	105622615	105622616	A	G	35	GENIC	homozygous	116837363
10	105623440	105623441	T	C	34	GENIC	homozygous	116837365
10	105623836	105623837	C	T	32	GENIC	homozygous	118088396