chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	74976784	74976785	C	T	73	GENIC	homozygous	139344629
13	74976882	74976883	A	G	58	GENIC	possibly homozygous	139344630
13	74977825	74977826	T	C	44	GENIC	homozygous	139344631
13	74977869	74977870	A	G	58	GENIC	homozygous	139344632
13	74977929	74977930	T	C	57	GENIC	homozygous	139344633
13	74978175	74978176	T	C	53	GENIC	homozygous	139344634
13	74979168	74979169	A	G	50	GENIC	homozygous	139344635
13	74979318	74979319	A	G	47	GENIC	homozygous	139344636
13	74980738	74980739	A		65	GENIC	homozygous	139184583
13	74982210	74982211	C	T	56	GENIC	homozygous	139344637
13	74983076	74983077	C	T	57	GENIC	homozygous	139344638
13	74983949	74983950	T	G	56	GENIC	homozygous	139344639
13	74984122	74984122		T	50	GENIC	homozygous	139184584
13	74985245	74985246	G	T	52	GENIC	homozygous	139344640
13	74985274	74985275	G	A	48	GENIC	homozygous	139344641
13	74985366	74985367	C	T	50	GENIC	homozygous	139344642
13	74985855	74985856	T		46	GENIC	possibly homozygous	139184585
13	74986282	74986283	A	C	62	GENIC	homozygous	139344643
13	74986303	74986304	T	C	57	GENIC	homozygous	139344644
13	74986335	74986336	A	C	56	GENIC	homozygous	139344645