chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39852731	39852732	C	A	21	GENIC	homozygous	116463578
8	39852884	39852888	ATTT		18	GENIC	homozygous	128585009
8	39853608	39853608		G	24	GENIC	homozygous	128585010
8	39854935	39854935		TTA	14	GENIC	homozygous	128585011
8	39860911	39860912	C	T	23	GENIC	homozygous	116463579
8	39860966	39860967	G	A	23	GENIC	homozygous	116463580
8	39861678	39861679	T	C	24	GENIC	homozygous	116463581
8	39862060	39862060		GAT	4	GENIC	homozygous	128585012
8	39862093	39862097	TGGA		7	GENIC	homozygous	128585013
8	39862502	39862503	G	C	15	GENIC	possibly homozygous	116463586
8	39863560	39863560		A	16	GENIC	homozygous	128585015
8	39863925	39863926	T	C	19	GENIC	homozygous	116463587
8	39864208	39864209	C	T	14	GENIC	homozygous	116463588
8	39864249	39864250	A	T	9	GENIC	homozygous	116463589
8	39864570	39864571	G	T	28	GENIC	homozygous	116463590
8	39864588	39864589	C	G	24	GENIC	homozygous	116463591
8	39864643	39864644	G	C	21	GENIC	homozygous	116463592
8	39865481	39865482	T		18	GENIC	homozygous	128585016
8	39866176	39866177	A	G	20	GENIC	homozygous	116463593
8	39866682	39866683	C	G	21	GENIC	homozygous	116463594