chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120950457	120950458	T	C	17	GENIC	homozygous	115857546
7	120950846	120950847	A	G	20	GENIC	homozygous	116409664
7	120951346	120951347	C	T	20	GENIC	homozygous	115857550
7	120951675	120951676	G	A	40	GENIC	homozygous	116409665
7	120953218	120953219	A	G	25	GENIC	homozygous	115857552
7	120953370	120953371	T	G	31	GENIC	homozygous	115857556
7	120954700	120954701	G	A	20	GENIC	homozygous	116409667
7	120954749	120954750	T	C	20	GENIC	homozygous	115857560
7	120955110	120955111	C	T	31	GENIC	homozygous	116409668
7	120956295	120956296	T	C	40	GENIC	homozygous	115857566
7	120956398	120956399	C	T	28	GENIC	homozygous	116409669
7	120957744	120957745	T	C	27	GENIC	homozygous	115857576
7	120957801	120957802	C	T	38	GENIC	homozygous	116409670
7	120959019	120959020	C	T	27	GENIC	homozygous	116409671
7	120959143	120959144	A	G	32	GENIC	homozygous	116409672
7	120960257	120960258	A	T	26	GENIC	homozygous	115857588
7	120960616	120960617	G	A	18	GENIC	homozygous	115857594
7	120960771	120960772	T	C	28	GENIC	homozygous	115857596
7	120961116	120961117	G	A	21	GENIC	homozygous	116409676
7	120961204	120961205	A	G	39	GENIC	homozygous	115857598
7	120961572	120961573	C	T	20	GENIC	homozygous	115857602
7	120962172	120962173	T	C	22	GENIC	homozygous	115857606
7	120965221	120965222	G	A	36	GENIC	homozygous	116409677