chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	79696845	79696846	T	G	16	GENIC	possibly homozygous	50106988
13	79697213	79697214	G	A	17	GENIC	possibly homozygous	50106990
13	79697405	79697406	A	G	13	GENIC	homozygous	50106992
13	79703698	79703699	T	C	25	GENIC	possibly homozygous	50106996
13	79704852	79704853	C	A	20	GENIC	homozygous	50106998
13	79707153	79707154	C	T	14	GENIC	possibly homozygous	50107000
13	79707195	79707196	C	CATGGTGT	2	GENIC	homozygous	50107002
13	79707377	79707378	A	-	11	GENIC	homozygous	50107004
13	79707721	79707722	G	T	9	GENIC	homozygous	49832463
13	79707723	79707727	TAAC	----	9	GENIC	homozygous	49832464
13	79708233	79708237	AACC	----	4	GENIC	homozygous	50107006
13	79708422	79708423	C	T	5	GENIC	heterozygous	50107008
13	79708423	79708424	A	G	5	GENIC	heterozygous	50107010
13	79708468	79708469	C	A	4	GENIC	homozygous	50107012
13	79708478	79708479	A	C	5	GENIC	homozygous	50107014
13	79708581	79708582	A	G	18	GENIC	homozygous	50107016
13	79709884	79709885	A	-	14	GENIC	possibly homozygous	50107018
13	79709978	79709979	A	G	14	GENIC	homozygous	50107020
13	79710143	79710144	A	G	13	GENIC	homozygous	50107022
13	79710667	79710668	T	C	16	GENIC	possibly homozygous	50107024
13	79710863	79710864	A	G	6	GENIC	homozygous	50107026
13	79711303	79711304	C	G	7	GENIC	possibly homozygous	49832466
13	79712213	79712214	A	G	11	GENIC	heterozygous	50107030
13	79712936	79712937	T	C	9	GENIC	homozygous	50107032
13	79714402	79714403	C	T	12	GENIC	homozygous	50107034
13	79714942	79714943	G	A	19	GENIC	possibly homozygous	50107036
13	79716646	79716647	C	-	5	GENIC	homozygous	49832468
13	79714977	79714978	T	C	21	GENIC	homozygous	50107038
13	79716282	79716283	C	A	11	GENIC	homozygous	50107044