chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	22750834	22750835	A	G	39	GENIC	homozygous	115282686
12	22752988	22752989	T	C	27	GENIC	homozygous	115282688
12	22753130	22753131	T	G	39	GENIC	homozygous	115282690
12	22753538	22753539	A	G	36	GENIC	homozygous	115282692
12	22753576	22753577	G	A	25	GENIC	homozygous	115282694
12	22754656	22754657	T	C	21	GENIC	homozygous	115282696
12	22754680	22754681	C	A	24	GENIC	homozygous	115282698
12	22754796	22754797	T	C	14	GENIC	homozygous	115282700
12	22755123	22755124	C	T	28	GENIC	homozygous	115282702
12	22755208	22755209	C	G	36	GENIC	homozygous	115282704
12	22755857	22755858	T	C	43	GENIC	homozygous	115282706
12	22755893	22755894	G	A	30	GENIC	homozygous	115282708
12	22757055	22757056	G	C	24	GENIC	homozygous	115282710
12	22761717	22761718	A	G	22	GENIC	homozygous	115282715
12	22759842	22759843	A	T	16	GENIC	homozygous	115367052
12	22763059	22763060	C	T	36	GENIC	homozygous	115282717
12	22763188	22763189	A	G	38	GENIC	homozygous	115282719
12	22763850	22763851	T	C	22	GENIC	homozygous	115282721
12	22763925	22763926	T	C	23	GENIC	homozygous	115282723
12	22764016	22764017	C	G	30	GENIC	homozygous	115282725
12	22764193	22764194	A	C	30	GENIC	homozygous	115282727
12	22764201	22764202	C	T	29	GENIC	homozygous	115282729