chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	107827037	107827038	C	T	16	GENIC	homozygous	116986151
8	107827950	107827951	C	T	21	GENIC	homozygous	116632870
8	107828356	107828357	A	G	15	GENIC	homozygous	116986153
8	107828560	107828561	T	C	25	GENIC	homozygous	116632874
8	107829040	107829041	A	G	14	GENIC	homozygous	116986154
8	107830412	107830413	G	A	19	GENIC	homozygous	116986156
8	107830434	107830435	G	T	15	GENIC	possibly homozygous	116986157
8	107830684	107830685	A	C	20	GENIC	homozygous	116986158
8	107831300	107831301	C	T	28	GENIC	homozygous	116986159
8	107831341	107831342	T	C	14	GENIC	homozygous	116986160
8	107832145	107832146	G	A	7	GENIC	homozygous	116986161
8	107832158	107832159	C	T	7	GENIC	homozygous	116986162
8	107832496	107832497	C	T	19	GENIC	homozygous	116986163
8	107832719	107832720	A	G	12	GENIC	homozygous	116986164
8	107832904	107832905	A	G	25	GENIC	homozygous	116632878
8	107833474	107833475	A	G	22	GENIC	homozygous	116986165
8	107834093	107834094	C	A	15	GENIC	homozygous	116986166
8	107834695	107834696	T	A	17	GENIC	homozygous	116986167
8	107834757	107834758	C	T	21	GENIC	homozygous	116986168
8	107834834	107834835	C	G	9	GENIC	homozygous	116986169
8	107835695	107835696	T	C	19	GENIC	homozygous	116632888
8	107835789	107835790	G	A	13	GENIC	homozygous	116986170
8	107836840	107836841	T	C	15	GENIC	homozygous	116632892
8	107836933	107836934	T	C	16	GENIC	homozygous	116986171
8	107836977	107836978	A	G	18	GENIC	homozygous	116632894
8	107838028	107838029	G	A	23	GENIC	homozygous	116986172
8	107838120	107838121	C	T	25	GENIC	homozygous	116986173