chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	19101354	19101355	T	C	59	GENIC	homozygous	139889623
16	19101713	19101714	G	A	66	GENIC	homozygous	139889624
16	19101865	19101866	G	A	50	GENIC	homozygous	139889625
16	19103548	19103549	C	T	11	GENIC	homozygous	139889626
16	19103557	19103558	T	C	11	GENIC	homozygous	139889627
16	19103698	19103699	C	T	33	GENIC	homozygous	139889628
16	19103834	19103835	C	G	44	GENIC	possibly homozygous	139889629
16	19103992	19103993	T	C	65	GENIC	homozygous	139889630
16	19104220	19104221	A	T	51	GENIC	homozygous	139889631
16	19104323	19104324	G	A	60	GENIC	homozygous	139889632
16	19104745	19104746	C	T	59	GENIC	homozygous	139889633
16	19105348	19105349	G	A	49	GENIC	homozygous	139889634
16	19105928	19105929	A	G	66	GENIC	homozygous	139889635
16	19106002	19106003	C	T	66	GENIC	homozygous	139889636
16	19106396	19106397	C	A	62	GENIC	homozygous	139889637
16	19106705	19106706	T	A	62	GENIC	homozygous	139889638
16	19107002	19107003	C	T	58	GENIC	homozygous	139889639
16	19107287	19107288	G	A	68	GENIC	homozygous	139889640
16	19107358	19107359	C	T	48	GENIC	homozygous	139889641
16	19108228	19108229	C	T	52	GENIC	homozygous	139889642
16	19103313	19103317	TCCT		45	GENIC	homozygous	139824778
16	19103482	19103488	CTCCTA		11	GENIC	homozygous	139824779
16	19103519	19103528	TCCTCCTCT		11	GENIC	homozygous	139824780
16	19103561	19103564	TCC		11	GENIC	homozygous	139824781
16	19103582	19103588	TCTTCC		8	GENIC	homozygous	139824782
16	19109539	19109539		A	50	GENIC	possibly homozygous	139824783