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	34	GENIC	homozygous	115282688
12	22753130	22753131	T	G	37	GENIC	homozygous	115282690
12	22753538	22753539	A	G	31	GENIC	homozygous	115282692
12	22753576	22753577	G	A	42	GENIC	homozygous	115282694
12	22754656	22754657	T	C	30	GENIC	homozygous	115282696
12	22754680	22754681	C	A	28	GENIC	homozygous	115282698
12	22754796	22754797	T	C	24	GENIC	homozygous	115282700
12	22755123	22755124	C	T	40	GENIC	homozygous	115282702
12	22755208	22755209	C	G	34	GENIC	homozygous	115282704
12	22755857	22755858	T	C	53	GENIC	homozygous	115282706
12	22755893	22755894	G	A	51	GENIC	homozygous	115282708
12	22757055	22757056	G	C	25	GENIC	homozygous	115282710
12	22760529	22760530	T	C	23	GENIC	homozygous	115282712
12	22761479	22761480	T	C	18	GENIC	homozygous	115282714
12	22761717	22761718	A	G	19	GENIC	homozygous	115282715
12	22763059	22763060	C	T	35	GENIC	homozygous	115282717
12	22763188	22763189	A	G	55	GENIC	homozygous	115282719
12	22763850	22763851	T	C	47	GENIC	homozygous	115282721
12	22763925	22763926	T	C	58	GENIC	homozygous	115282723
12	22764016	22764017	C	G	51	GENIC	homozygous	115282725
12	22764193	22764194	A	C	42	GENIC	homozygous	115282727
12	22764201	22764202	C	T	44	GENIC	homozygous	115282729