chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90224332	90224333	C	T	34	GENIC	homozygous	66590277
13	90225422	90225423	G	A	14	GENIC	possibly homozygous	66374531
13	90225683	90225684	T	A	2	GENIC	homozygous	66374533
13	90225271	90225272	A	G	13	GENIC	heterozygous	66374527
13	90225286	90225287	G	A	13	GENIC	homozygous	66374529
13	90225765	90225766	T	C	4	GENIC	homozygous	66374535
13	90225768	90225769	C	T	4	GENIC	homozygous	66374537
13	90226146	90226147	G	A	10	GENIC	homozygous	66374539
13	90226402	90226403	T	C	18	GENIC	homozygous	66374541
13	90226952	90226953	T	G	31	GENIC	homozygous	66374543
13	90227500	90227501	G	A	13	GENIC	homozygous	66374545
13	90227721	90227722	G	A	31	GENIC	homozygous	66374547
13	90228499	90228500	C	T	28	GENIC	homozygous	66374549
13	90229613	90229614	C	A	26	GENIC	homozygous	66374551
13	90230679	90230680	C	T	21	GENIC	homozygous	66374553
13	90234292	90234293	T	G	28	GENIC	homozygous	66374555
13	90235223	90235224	C	T	33	GENIC	homozygous	66374557
13	90235442	90235443	G	T	28	GENIC	homozygous	66374559
13	90236528	90236529	A	T	39	GENIC	homozygous	66374561
13	90236671	90236672	G	A	52	GENIC	homozygous	66374563
13	90237704	90237705	A	G	22	GENIC	homozygous	66374565
13	90238329	90238330	C	A	19	GENIC	homozygous	66374567
13	90239184	90239185	C	T	39	GENIC	homozygous	66374569