chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90943522	90943523	A	C	34	GENIC	heterozygous	118536807
13	90943703	90943704	G	A	35	GENIC	homozygous	114575409
13	90944492	90944493	T	C	29	GENIC	homozygous	114575411
13	90944643	90944644	G	C	20	GENIC	homozygous	114575413
13	90944781	90944782	C	G	30	GENIC	homozygous	114575415
13	90945225	90945226	A	G	25	GENIC	homozygous	114575417
13	90945573	90945574	T	C	31	GENIC	homozygous	114649416
13	90945859	90945860	A	G	28	GENIC	homozygous	114649418
13	90946100	90946101	T	C	33	GENIC	homozygous	114649420
13	90946339	90946340	A	C	16	GENIC	homozygous	114575419
13	90947189	90947190	T	A	42	GENIC	heterozygous	118536808
13	90947805	90947806	C	T	30	GENIC	homozygous	114575423
13	90947986	90947987	G	T	42	GENIC	homozygous	114575425
13	90948905	90948906	T	C	22	GENIC	homozygous	114575427
13	90949435	90949436	T	A	33	GENIC	homozygous	114575429
13	90949506	90949507	T	G	31	GENIC	homozygous	114575431
13	90949607	90949608	G	A	36	GENIC	homozygous	114575432
13	90951287	90951288	T	G	32	GENIC	homozygous	114575434
13	90947168	90947169	C	G	41	GENIC	heterozygous	118528973
13	90946853	90946854	C	G	37	GENIC	heterozygous	118528971
13	90947074	90947075	C	T	53	GENIC	heterozygous	118528972