chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	61249719	61249720	G	C	15	GENIC	homozygous	48747793
14	61251344	61251345	A	G	24	GENIC	homozygous	48747795
14	61251880	61251881	C	T	19	GENIC	homozygous	48747797
14	61252066	61252067	G	-	29	GENIC	homozygous	48747799
14	61252074	61252075	G	-	29	GENIC	homozygous	48747801
14	61252077	61252078	C	-	28	GENIC	homozygous	48747803
14	61256939	61256940	A	G	27	GENIC	homozygous	48747805
14	61260725	61260726	A	C	14	GENIC	homozygous	49311072
14	61260727	61260728	T	A	14	GENIC	homozygous	49311073
14	61260738	61260739	C	-	16	GENIC	homozygous	48747807
14	61260742	61260743	C	T	16	GENIC	homozygous	49311074
14	61260745	61260746	T	-	16	GENIC	homozygous	48747809
14	61260749	61260750	C	G	14	GENIC	homozygous	48747811
14	61260755	61260756	A	T	14	GENIC	homozygous	48747813
14	61260758	61260759	C	G	14	GENIC	homozygous	48747815
14	61260764	61260765	A	-	16	GENIC	homozygous	48747817
14	61260768	61260769	C	-	16	GENIC	homozygous	48747818
14	61260774	61260775	A	-	15	GENIC	homozygous	48747820
14	61260781	61260782	G	-	17	GENIC	homozygous	48747822
14	61260810	61260811	T	TA	22	GENIC	homozygous	48747824
14	61260814	61260816	AA	--	22	GENIC	homozygous	48747826
14	61263292	61263293	C	T	3	GENIC	homozygous	48747828
14	61275911	61275912	C	T	20	GENIC	homozygous	48747829
14	61276438	61276439	T	C	21	GENIC	homozygous	48747831
14	61278402	61278403	A	-	28	GENIC	homozygous	48747833
14	61279097	61279098	T	-	15	GENIC	heterozygous	49422838
14	61279230	61279231	A	-	15	GENIC	homozygous	48747835
14	61279605	61279606	C	CCCTCTTGTCTTACAGATGTGGTTAGGT	39	GENIC	homozygous	48747839
14	61282872	61282873	A	-	10	GENIC	possibly homozygous	48747841
14	61284068	61284069	A	G	33	GENIC	homozygous	48747843
14	61285639	61285640	G	A	21	GENIC	homozygous	48747845
14	61286277	61286278	C	G	18	GENIC	homozygous	48747847
14	61286313	61286315	CC	--	7	GENIC	heterozygous	49311075
14	61286314	61286315	C	-	7	GENIC	heterozygous	49326086
14	61260783	61260784	A	T	17	GENIC	homozygous	49288793