chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	19097968	19097969	C	T	37	GENIC	homozygous	145884854
16	19102194	19102195	C	T	13	GENIC	homozygous	145884855
16	19101865	19101866	G	A	25	GENIC	homozygous	139889625
16	19101354	19101355	T	C	16	GENIC	homozygous	139889623
16	19101713	19101714	G	A	31	GENIC	homozygous	139889624
16	19102967	19102967		GGAGGGAA	6	GENIC	heterozygous	145880866
16	19103546	19103546		TCT	7	GENIC	homozygous	145880867
16	19102971	19102971		GGAA	7	GENIC	heterozygous	148118109
16	19103313	19103317	TCCT		20	GENIC	homozygous	139824778
16	19103519	19103528	TCCTCCTCT		7	GENIC	homozygous	139824780
16	19103698	19103699	C	T	21	GENIC	homozygous	139889628
16	19103834	19103835	C	G	26	GENIC	homozygous	139889629
16	19103992	19103993	T	C	16	GENIC	homozygous	139889630
16	19104220	19104221	A	T	18	GENIC	homozygous	139889631
16	19104323	19104324	G	A	37	GENIC	homozygous	139889632
16	19104745	19104746	C	T	27	GENIC	possibly homozygous	139889633
16	19105348	19105349	G	A	28	GENIC	homozygous	139889634
16	19105928	19105929	A	G	14	GENIC	homozygous	139889635
16	19106002	19106003	C	T	19	GENIC	homozygous	139889636
16	19106396	19106397	C	A	19	GENIC	homozygous	139889637
16	19107002	19107003	C	T	29	GENIC	homozygous	139889639
16	19107177	19107178	G	A	32	GENIC	homozygous	145884856
16	19107287	19107288	G	A	33	GENIC	homozygous	139889640
16	19107358	19107359	C	T	26	GENIC	homozygous	139889641
16	19110431	19110432	G	A	14	GENIC	homozygous	145884857