chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105618960	105618961	A	G	26	GENIC	homozygous	116837329
10	105620069	105620070	A	G	18	GENIC	homozygous	116837331
10	105620227	105620228	T	A	15	GENIC	homozygous	116837333
10	105620284	105620285	C	T	13	GENIC	homozygous	116837337
10	105620528	105620529	A	G	25	GENIC	homozygous	116837339
10	105621079	105621080	A	G	13	GENIC	homozygous	117031771
10	105621430	105621431	A	G	32	GENIC	homozygous	116837341
10	105621556	105621557	G	A	26	GENIC	homozygous	116837343
10	105621779	105621780	T	G	24	GENIC	homozygous	116837345
10	105621781	105621782	C	G	23	GENIC	homozygous	116837347
10	105621815	105621816	G	T	22	GENIC	homozygous	116837349
10	105622175	105622176	A	G	28	GENIC	homozygous	116837351
10	105622205	105622206	T	C	25	GENIC	homozygous	116837353
10	105622209	105622210	A	C	21	GENIC	homozygous	116837355
10	105622279	105622280	C	T	27	GENIC	homozygous	117031773
10	105622320	105622321	T	C	14	GENIC	homozygous	117031775
10	105622337	105622338	A	G	22	GENIC	homozygous	116837357
10	105622412	105622413	A	T	18	GENIC	homozygous	116837359
10	105622421	105622422	G	T	19	GENIC	homozygous	116837361
10	105622615	105622616	A	G	22	GENIC	homozygous	116837363
10	105623440	105623441	T	C	26	GENIC	homozygous	116837365