chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	71058111	71058112	C	G	34	GENIC	homozygous	112025401
16	71058698	71058699	G	C	28	GENIC	homozygous	111855025
16	71058699	71058700	C	G	28	GENIC	homozygous	111855026
16	71058730	71058731	C	T	26	GENIC	homozygous	111855027
16	71060085	71060086	C	T	32	GENIC	homozygous	112025405
16	71060230	71060231	T	G	36	GENIC	homozygous	112025407
16	71060232	71060233	G	C	38	GENIC	homozygous	112025409
16	71060521	71060522	G	A	20	GENIC	homozygous	112025411
16	71060577	71060578	T	C	30	GENIC	homozygous	112025413
16	71061506	71061507	T	C	32	GENIC	homozygous	112025415
16	71062490	71062491	G	A	60	GENIC	homozygous	112025417
16	71065308	71065309	G	T	18	GENIC	homozygous	111855033
16	71065309	71065310	T	G	18	GENIC	homozygous	111855034
16	71066578	71066579	A	G	16	GENIC	homozygous	112025419
16	71070656	71070657	C	T	20	GENIC	homozygous	112025421
16	71066081	71066082	G	A	23	GENIC	homozygous	112313092
16	71071573	71071574	G	A	13	GENIC	homozygous	112025423
16	71071899	71071900	C	A	43	GENIC	homozygous	112025425
16	71072835	71072836	G	A	35	GENIC	homozygous	112025427