chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	111835770	111835771	T	C	25	GENIC	homozygous	59021738
2	111835791	111835792	G	T	23	GENIC	homozygous	59021739
2	111835826	111835827	A	AC	22	GENIC	homozygous	59021740
2	111835908	111835909	C	T	19	GENIC	homozygous	59021741
2	111836059	111836060	T	C	33	GENIC	homozygous	59021742
2	111836218	111836219	T	G	34	GENIC	homozygous	59021743
2	111836860	111836861	T	A	24	GENIC	homozygous	59021744
2	111837033	111837034	C	T	21	GENIC	homozygous	59021745
2	111837055	111837056	T	C	34	GENIC	homozygous	59021746
2	111837056	111837057	C	T	33	GENIC	homozygous	59021747
2	111837531	111837532	A	C	33	GENIC	homozygous	59021748
2	111837554	111837555	T	C	29	GENIC	homozygous	59021749
2	111837855	111837856	G	A	30	GENIC	homozygous	59021750
2	111838008	111838009	T	G	27	GENIC	homozygous	59021751
2	111838338	111838339	T	C	24	GENIC	homozygous	59021752
2	111838463	111838464	T	C	5	GENIC	homozygous	59021753
2	111838660	111838661	C	A	16	GENIC	homozygous	59021754
2	111839273	111839274	G	T	12	GENIC	homozygous	59021755
2	111839692	111839693	T	C	13	GENIC	homozygous	59021756
2	111839973	111839974	C	T	8	GENIC	homozygous	59021757
2	111840740	111840741	T	C	18	GENIC	homozygous	59021758
2	111841130	111841131	C	T	18	GENIC	homozygous	59021759
2	111841151	111841152	T	G	16	GENIC	homozygous	59021760
2	111841706	111841707	T	C	33	GENIC	homozygous	59021762
2	111841936	111841937	C	T	28	GENIC	homozygous	59021763
2	111842216	111842217	C	A	29	GENIC	homozygous	59021764
2	111841605	111841608	CTG	---	16	GENIC	homozygous	60493898