chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	140845519	140845520	G	A	23	GENIC	homozygous	108259022
1	140846341	140846342	C	T	36	GENIC	homozygous	108936361
1	140847133	140847134	A	C	28	GENIC	homozygous	108936362
1	140847185	140847186	G	A	21	GENIC	homozygous	108936363
1	140847446	140847447	G	A	35	GENIC	homozygous	108936364
1	140847676	140847677	C	T	22	GENIC	homozygous	108936365
1	140848190	140848191	T	C	69	GENIC	homozygous	108936366
1	140848394	140848395	C	T	31	GENIC	homozygous	108936367
1	140848827	140848828	C	T	28	GENIC	homozygous	108936368
1	140849120	140849121	C	A	32	GENIC	homozygous	109048848
1	140849499	140849500	G	A	41	GENIC	homozygous	108259034
1	140850550	140850551	G	T	39	GENIC	homozygous	108259035
1	140850659	140850660	G	A	27	GENIC	homozygous	108259037
1	140851129	140851130	C	T	16	GENIC	homozygous	108259039
1	140851141	140851142	A	T	15	GENIC	homozygous	108259041
1	140851469	140851470	T	C	32	GENIC	homozygous	108259043
1	140855002	140855003	A	G	39	GENIC	homozygous	108259049
1	140855711	140855712	C	T	21	GENIC	homozygous	108259051
1	140857565	140857566	T	C	33	GENIC	homozygous	108259053
1	140858263	140858264	G	C	34	GENIC	homozygous	108259055
1	140858312	140858313	A	C	28	GENIC	homozygous	108259057