chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	61569913	61569914	A	G	31	GENIC	homozygous	49777442
13	61571425	61571426	C	CTTTT	9	GENIC	homozygous	50564474
13	61571464	61571465	T	-	11	GENIC	heterozygous	50595329
13	61571604	61571605	G	-	43	GENIC	homozygous	49777445
13	61573502	61573508	GATGAC	------	8	GENIC	homozygous	49777446
13	61574207	61574208	T	A	40	GENIC	homozygous	49777448
13	61574239	61574240	T	C	31	GENIC	homozygous	49777449
13	61574310	61574311	T	TC	33	GENIC	homozygous	49777450
13	61574311	61574312	T	TGGTGGTTC	34	GENIC	homozygous	49777451
13	61581329	61581330	T	-	14	GENIC	homozygous	49777453
13	61585396	61585399	TTT	---	3	GENIC	heterozygous	50605733
13	61590365	61590366	T	C	42	GENIC	homozygous	49777462
13	61591028	61591029	G	C	13	GENIC	homozygous	49777463
13	61591063	61591064	C	T	21	GENIC	homozygous	49777464
13	61591243	61591244	A	AT	23	GENIC	homozygous	49777465
13	61591291	61591292	C	A	33	GENIC	homozygous	49777466
13	61591294	61591295	C	T	34	GENIC	homozygous	49777467
13	61591319	61591320	C	T	44	GENIC	homozygous	49777468
13	61591379	61591380	G	C	51	GENIC	homozygous	49777469
13	61591509	61591510	C	T	49	GENIC	homozygous	49777473
13	61591736	61591737	C	T	39	GENIC	homozygous	49777474
13	61592022	61592023	A	T	15	GENIC	homozygous	49777475
13	61595584	61595585	T	C	51	GENIC	homozygous	49777476
13	61596962	61596963	G	A	40	GENIC	homozygous	49777477
13	61598221	61598222	G	A	35	GENIC	homozygous	49777478
13	61598829	61598830	G	A	50	GENIC	homozygous	49777479
13	61602415	61602416	C	T	33	GENIC	homozygous	49777480
13	61604203	61604207	AAGT	----	22	GENIC	homozygous	49777482
13	61584838	61584839	G	GT	6	GENIC	heterozygous	50654425
13	61591429	61591430	C	CAAAG	60	GENIC	homozygous	50495749
13	61591432	61591433	A	AAAGGAAAG	62	GENIC	homozygous	50495750