chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	126573813	126573814	A	G	12	GENIC	homozygous	108220444
1	126574023	126574024	T	C	9	GENIC	homozygous	108220446
1	126576724	126576725	A	G	4	GENIC	homozygous	108220450
1	126576920	126576921	T	G	31	GENIC	homozygous	108220452
1	126577122	126577123	T	C	19	GENIC	possibly homozygous	108220454
1	126577265	126577266	C	T	25	GENIC	homozygous	108220456
1	126577324	126577325	A	T	18	GENIC	homozygous	108220458
1	126577803	126577804	G	T	12	GENIC	homozygous	108926300
1	126577821	126577822	G	T	16	GENIC	homozygous	108220460
1	126577909	126577910	T	C	14	GENIC	homozygous	108220462
1	126578055	126578056	T	C	19	GENIC	homozygous	108220464
1	126578143	126578144	G	A	16	GENIC	homozygous	108926301
1	126578222	126578223	A	G	22	GENIC	homozygous	108220466
1	126579215	126579216	C	T	16	GENIC	homozygous	120671035
1	126579396	126579397	A	G	13	GENIC	homozygous	108220470
1	126579422	126579423	T	C	10	GENIC	homozygous	108220472
1	126579685	126579686	T	G	10	GENIC	homozygous	108220474
1	126579696	126579697	T	C	8	GENIC	homozygous	108220476
1	126581261	126581262	C	T	7	GENIC	homozygous	120671037
1	126587346	126587347	C	T	14	GENIC	homozygous	108220484
1	126588163	126588164	T	C	29	GENIC	homozygous	108220486