chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	19101354	19101355	T	C	23	GENIC	homozygous	139889623
16	19101713	19101714	G	A	24	GENIC	homozygous	139889624
16	19101865	19101866	G	A	25	GENIC	homozygous	139889625
16	19103313	19103317	TCCT		29	GENIC	homozygous	139824778
16	19103482	19103488	CTCCTA		12	GENIC	homozygous	139824779
16	19103519	19103528	TCCTCCTCT		12	GENIC	homozygous	139824780
16	19103548	19103549	C	T	12	GENIC	homozygous	139889626
16	19103557	19103558	T	C	12	GENIC	homozygous	139889627
16	19103561	19103564	TCC		12	GENIC	homozygous	139824781
16	19103582	19103588	TCTTCC		9	GENIC	homozygous	139824782
16	19103698	19103699	C	T	17	GENIC	homozygous	139889628
16	19103834	19103835	C	G	20	GENIC	homozygous	139889629
16	19103992	19103993	T	C	19	GENIC	homozygous	139889630
16	19104220	19104221	A	T	20	GENIC	homozygous	139889631
16	19104323	19104324	G	A	18	GENIC	homozygous	139889632
16	19104745	19104746	C	T	22	GENIC	homozygous	139889633
16	19106002	19106003	C	T	22	GENIC	homozygous	139889636
16	19105348	19105349	G	A	21	GENIC	homozygous	139889634
16	19105928	19105929	A	G	20	GENIC	homozygous	139889635
16	19106396	19106397	C	A	23	GENIC	homozygous	139889637
16	19106705	19106706	T	A	16	GENIC	homozygous	139889638
16	19107002	19107003	C	T	19	GENIC	homozygous	139889639
16	19107287	19107288	G	A	25	GENIC	homozygous	139889640
16	19107358	19107359	C	T	15	GENIC	homozygous	139889641
16	19108228	19108229	C	T	17	GENIC	homozygous	139889642
16	19109539	19109539		A	15	GENIC	homozygous	139824783