chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116503819	116503820	C	T	8	GENIC	homozygous	116669509
8	116504170	116504171	G	A	2	GENIC	homozygous	116669513
8	116504177	116504178	G	T	3	GENIC	homozygous	116669515
8	116505381	116505382	C	G	23	GENIC	homozygous	116669519
8	116506383	116506384	A	G	27	GENIC	homozygous	116669521
8	116507109	116507110	C	A	30	GENIC	homozygous	116669523
8	116507114	116507115	A	T	25	GENIC	homozygous	116669525
8	116507184	116507185	G	C	20	GENIC	homozygous	116669527
8	116507503	116507504	C	T	23	GENIC	homozygous	116669529
8	116508127	116508128	T	C	14	GENIC	homozygous	116669539
8	116514226	116514227	A	G	28	GENIC	homozygous	116669543
8	116514882	116514883	A	G	36	GENIC	homozygous	116669545
8	116519326	116519327	G	A	16	GENIC	homozygous	116669549
8	116519454	116519455	C	T	17	GENIC	homozygous	116669551
8	116520058	116520059	A	G	25	GENIC	homozygous	116669553
8	116520078	116520079	C	T	28	GENIC	homozygous	116669555
8	116521963	116521964	T	C	33	GENIC	homozygous	116669557
8	116523112	116523113	C	G	29	GENIC	homozygous	116669559
8	116525823	116525824	C	T	19	GENIC	homozygous	116669565
8	116526281	116526282	C	T	7	GENIC	homozygous	116669567
8	116528281	116528282	G	C	4	GENIC	homozygous	116669569
8	116529571	116529572	T	C	26	GENIC	homozygous	116669571
8	116529845	116529846	C	T	30	GENIC	homozygous	116669575
8	116530262	116530263	C	T	13	GENIC	homozygous	116669577
8	116531167	116531168	T	A	16	GENIC	homozygous	116669579
8	116532097	116532098	G	A	4	GENIC	homozygous	116669581