chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52990869	52990870	G	T	14	GENIC	possibly homozygous	50361712
13	52991390	52991391	C	A	19	GENIC	homozygous	50361714
13	52991800	52991801	T	C	10	GENIC	possibly homozygous	50361716
13	52991853	52991854	T	TGG	10	GENIC	possibly homozygous	50361718
13	52991938	52991939	A	T	25	GENIC	homozygous	49949130
13	52992176	52992177	G	GCATA	3	GENIC	heterozygous	49949131
13	52992263	52992264	G	-	4	GENIC	homozygous	50361720
13	52992267	52992270	GGG	---	5	GENIC	homozygous	50361724
13	52992300	52992301	T	C	5	GENIC	homozygous	50361726
13	52992310	52992311	G	GAA	2	GENIC	homozygous	50361728
13	52992511	52992512	T	C	18	GENIC	homozygous	50361730
13	52992745	52992746	T	C	14	GENIC	possibly homozygous	50361732
13	52992768	52992769	C	T	14	GENIC	possibly homozygous	50361734
13	52992847	52992848	G	C	5	GENIC	heterozygous	50361736
13	52992978	52992979	C	T	8	GENIC	heterozygous	50361738
13	52993775	52993776	T	TCC	7	GENIC	homozygous	50361740
13	52993822	52993826	TCCA	----	6	GENIC	heterozygous	50361742
13	52993974	52993975	T	C	17	GENIC	homozygous	50361744
13	52994599	52994600	T	C	20	GENIC	possibly homozygous	49949136
13	52994858	52994859	C	T	5	GENIC	homozygous	49949137
13	52995304	52995305	C	-	11	GENIC	possibly homozygous	49758389
13	52995558	52995559	A	G	22	GENIC	homozygous	50361746
13	52995581	52995582	G	A	21	GENIC	possibly homozygous	50361748
13	52995675	52995676	T	C	23	GENIC	possibly homozygous	50361750
13	52996154	52996155	A	G	7	GENIC	homozygous	50230688
13	52996196	52996197	C	T	11	GENIC	possibly homozygous	50230690
13	52996392	52996393	C	A	17	GENIC	heterozygous	50230692
13	52996449	52996450	G	A	15	GENIC	homozygous	50361752
13	52996506	52996507	C	G	9	GENIC	possibly homozygous	50361754
13	52996536	52996537	C	-	13	GENIC	homozygous	50361756
13	52997782	52997783	C	T	12	GENIC	possibly homozygous	50361758
13	52997884	52997885	T	TTG	2	GENIC	heterozygous	50230702
13	52998003	52998004	C	-	8	GENIC	heterozygous	49949140