chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47067387	47067388	T	C	27	GENIC	homozygous	116587179
10	47068507	47068508	A	G	24	GENIC	homozygous	116587183
10	47081680	47081681	C	T	33	GENIC	homozygous	117277964
10	47082373	47082374	G	A	21	GENIC	homozygous	116587185
10	47083081	47083082	G	A	35	GENIC	homozygous	116587187
10	47083672	47083673	T	C	29	GENIC	homozygous	116587189
10	47084322	47084323	A	G	30	GENIC	homozygous	116587191
10	47084461	47084462	T	C	21	GENIC	homozygous	116587193
10	47085873	47085874	T	C	21	GENIC	homozygous	116587197
10	47086422	47086423	G	C	25	GENIC	possibly homozygous	116587199
10	47086500	47086501	A	G	43	GENIC	homozygous	116587201
10	47086652	47086653	C	A	26	GENIC	homozygous	116587203
10	47087348	47087349	G	A	30	GENIC	homozygous	116587205
10	47089091	47089092	G	T	37	GENIC	homozygous	117253123
10	47089961	47089962	T	C	16	GENIC	homozygous	116587209
10	47091233	47091234	G	A	28	GENIC	homozygous	116587211
10	47091288	47091289	G	T	30	GENIC	homozygous	116587213
10	47091533	47091534	C	T	30	GENIC	homozygous	116587217
10	47092963	47092964	T	C	20	GENIC	homozygous	116587219
10	47093708	47093709	T	C	16	GENIC	homozygous	116587225
10	47093872	47093873	G	C	15	GENIC	homozygous	117277966
10	47093905	47093906	T	A	17	GENIC	homozygous	117178159
10	47095400	47095401	A	C	16	GENIC	homozygous	116587229
10	47096988	47096989	C	T	44	GENIC	homozygous	116587233
10	47097004	47097005	T	C	42	GENIC	homozygous	116587235
10	47097812	47097813	T	C	17	GENIC	homozygous	116587237
10	47098398	47098399	C	T	25	GENIC	homozygous	116587241
10	47101758	47101759	C	T	37	GENIC	homozygous	116587245