chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	127460075	127460076	C	T	30	GENIC	homozygous	110008595
2	127461248	127461249	C	G	30	GENIC	homozygous	110008596
2	127461426	127461427	C	T	32	GENIC	homozygous	110008597
2	127461736	127461737	G	C	46	GENIC	homozygous	110008598
2	127461737	127461738	T	C	47	GENIC	homozygous	110008599
2	127462095	127462096	C	G	28	GENIC	homozygous	110008600
2	127462492	127462493	T	G	23	GENIC	homozygous	110008601
2	127464321	127464322	C	T	31	GENIC	homozygous	110008603
2	127465664	127465665	G	T	33	GENIC	homozygous	110008605
2	127469602	127469603	C	T	39	GENIC	homozygous	110008611
2	127469706	127469707	T	C	36	GENIC	homozygous	110008612
2	127470313	127470314	C	T	51	GENIC	homozygous	110008613
2	127471677	127471678	G	A	39	GENIC	homozygous	110008614
2	127472276	127472277	G	A	48	GENIC	homozygous	110008615
2	127474207	127474208	G	C	37	GENIC	homozygous	110008617
2	127475369	127475370	A	T	48	GENIC	homozygous	110008618
2	127475578	127475579	A	G	48	GENIC	homozygous	110008619
2	127476609	127476610	C	T	47	GENIC	homozygous	110008622
2	127476699	127476700	C	T	45	GENIC	homozygous	110008623
2	127509892	127509893	G	A	43	GENIC	homozygous	110008627
2	127510889	127510890	A	G	39	GENIC	homozygous	110008628
2	127511296	127511297	T	C	52	GENIC	homozygous	110008629
2	127512305	127512306	T	C	17	GENIC	homozygous	110008630
2	127512789	127512790	T	A	33	GENIC	homozygous	110008631
2	127515095	127515096	T	G	51	GENIC	homozygous	110008632
2	127515196	127515197	T	C	53	GENIC	homozygous	110008633
2	127520202	127520203	T	C	21	GENIC	homozygous	110008636
2	127520305	127520306	C	G	49	GENIC	homozygous	110008637
2	127520516	127520517	G	A	22	GENIC	homozygous	110008638
2	127520894	127520895	C	A	16	GENIC	homozygous	110008639