chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	20910088	20910089	A	G	25	GENIC	homozygous	109630497
2	20910710	20910711	C	A	24	GENIC	homozygous	109630499
2	20910745	20910746	G	A	26	GENIC	homozygous	109630501
2	20910823	20910824	G	C	31	GENIC	homozygous	109630503
2	20910827	20910828	C	T	30	GENIC	homozygous	109630505
2	20911512	20911513	T	G	31	GENIC	homozygous	109630507
2	20912384	20912385	A	G	39	GENIC	homozygous	109630509
2	20914506	20914507	T	C	22	GENIC	homozygous	109630511
2	20914718	20914719	A	C	28	GENIC	homozygous	109630513
2	20914731	20914732	C	T	30	GENIC	homozygous	109630515
2	20914807	20914808	T	C	29	GENIC	homozygous	109630517
2	20914814	20914815	T	C	28	GENIC	homozygous	109630518
2	20914822	20914823	A	G	32	GENIC	homozygous	109630520
2	20914895	20914896	T	G	41	GENIC	homozygous	109630522
2	20914921	20914922	A	G	42	GENIC	homozygous	109630524
2	20915014	20915015	A	G	18	GENIC	homozygous	109630526
2	20915142	20915143	C	G	39	GENIC	homozygous	109630528
2	20916239	20916240	T	C	27	GENIC	homozygous	109630530
2	20916338	20916339	C	A	36	GENIC	homozygous	109630532
2	20916960	20916961	G	T	22	GENIC	homozygous	109630534
2	20917008	20917009	C	A	29	GENIC	homozygous	109630536
2	20917133	20917134	A	G	27	GENIC	homozygous	109630538
2	20917866	20917867	A	G	26	GENIC	homozygous	109630540
2	20919508	20919509	A	G	15	GENIC	homozygous	109630542