chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	20910088	20910089	A	G	22	GENIC	homozygous	109630497
2	20910094	20910095	C	T	22	GENIC	homozygous	110671771
2	20910710	20910711	C	A	19	GENIC	homozygous	109630499
2	20910745	20910746	G	A	16	GENIC	homozygous	109630501
2	20910823	20910824	G	C	23	GENIC	homozygous	109630503
2	20910827	20910828	C	T	22	GENIC	homozygous	109630505
2	20911345	20911346	C	T	32	GENIC	homozygous	110671773
2	20911512	20911513	T	G	28	GENIC	homozygous	109630507
2	20912384	20912385	A	G	29	GENIC	homozygous	109630509
2	20913119	20913120	G	A	21	GENIC	homozygous	110671775
2	20913427	20913428	C	T	29	GENIC	homozygous	110671777
2	20913565	20913566	C	T	24	GENIC	homozygous	110671778
2	20914807	20914808	T	C	31	GENIC	homozygous	109630517
2	20916123	20916124	C	T	20	GENIC	homozygous	110671780
2	20916960	20916961	G	T	22	GENIC	homozygous	109630534
2	20917133	20917134	A	G	38	GENIC	homozygous	109630538
2	20917866	20917867	A	G	29	GENIC	homozygous	109630540
2	20918032	20918033	G	A	27	GENIC	homozygous	110671782
2	20919508	20919509	A	G	13	GENIC	homozygous	109630542