chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	106630469	106630470	A	AT	7	GENIC	homozygous	49874241
13	106630955	106630956	G	A	25	GENIC	possibly homozygous	49977943
13	106631584	106631585	G	A	20	GENIC	homozygous	49977944
13	106631605	106631606	G	A	14	GENIC	homozygous	49977945
13	106631650	106631651	C	T	19	GENIC	heterozygous	49977946
13	106632934	106632935	C	-	17	GENIC	homozygous	49874242
13	106633824	106633825	T	-	14	GENIC	homozygous	49977950
13	106634189	106634194	GTTTT	-----	7	GENIC	heterozygous	49977951
13	106636261	106636262	A	-	4	GENIC	heterozygous	49977952
13	106636278	106636279	A	-	2	GENIC	homozygous	49977953
13	106637568	106637569	A	G	6	GENIC	heterozygous	49977955
13	106638644	106638645	T	A	20	GENIC	homozygous	49977957
13	106639210	106639211	C	T	15	GENIC	homozygous	49977958
13	106639563	106639564	T	-	13	GENIC	homozygous	49977959
13	106639805	106639806	A	G	4	GENIC	heterozygous	49977960
13	106640417	106640418	G	A	8	GENIC	heterozygous	49977969
13	106643966	106643967	G	A	17	GENIC	homozygous	49977970
13	106645097	106645111	TCTCAACTTGTGGG	--------------	6	GENIC	homozygous	49977974
13	106645486	106645487	C	T	9	GENIC	possibly homozygous	49977976
13	106645754	106645756	CA	--	11	GENIC	possibly homozygous	49977977
13	106646034	106646035	G	-	17	GENIC	homozygous	49977978
13	106646718	106646719	A	G	2	GENIC	homozygous	49977980
13	106646776	106646777	T	C	3	GENIC	homozygous	49977981
13	106646923	106646924	T	C	11	GENIC	homozygous	49977982
13	106647053	106647054	T	C	20	GENIC	homozygous	49977983
13	106647207	106647208	T	-	15	GENIC	homozygous	49977984
13	106647570	106647571	G	GAGAGGA	2	GENIC	heterozygous	50861431
13	106633408	106633409	T	TTAAAAA	3	GENIC	homozygous	50839466
13	106637767	106637768	T	TAAATAAATAAATAAATAAAA	5	GENIC	homozygous	50861425
13	106648034	106648035	A	-	11	GENIC	possibly homozygous	49977992
13	106648152	106648153	A	T	23	GENIC	homozygous	49977993
13	106648228	106648229	T	C	21	GENIC	possibly homozygous	49977994