chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	61453008	61453009	T	C	34	GENIC	homozygous	53931898
7	61453893	61453894	A	G	28	GENIC	homozygous	53931901
7	61453897	61453898	A	G	29	GENIC	homozygous	53931902
7	61456315	61456316	A	T	25	GENIC	homozygous	53931904
7	61453291	61453292	C	CTGTGTGTGTGTG	6	GENIC	heterozygous	55025150
7	61455991	61455992	T	TCAAACACACACACA	10	GENIC	homozygous	55218477
7	61453291	61453292	C	CTGTGTGTG	6	GENIC	heterozygous	55082089
7	61456962	61456963	T	C	38	GENIC	homozygous	53931905
7	61457219	61457220	A	C	31	GENIC	homozygous	53931906
7	61457435	61457436	T	C	39	GENIC	homozygous	53931907
7	61457492	61457493	T	A	30	GENIC	homozygous	53931908
7	61457577	61457578	T	A	29	GENIC	homozygous	53931909
7	61458103	61458104	C	A	30	GENIC	homozygous	53931910
7	61458269	61458279	TGTGTGTGTA	----------	21	GENIC	homozygous	53931911
7	61458653	61458654	G	GA	23	GENIC	possibly homozygous	53931913
7	61459479	61459481	TG	--	18	GENIC	homozygous	53931914
7	61459508	61459510	AT	--	23	GENIC	homozygous	53931915
7	61462445	61462446	A	G	18	GENIC	homozygous	53931916
7	61462552	61462553	A	C	15	GENIC	homozygous	53931917
7	61463315	61463316	A	G	40	GENIC	homozygous	53931918
7	61463350	61463351	G	A	48	GENIC	homozygous	53931919
7	61464332	61464333	G	-	22	GENIC	possibly homozygous	53931920
7	61464962	61464963	A	G	29	GENIC	homozygous	53931924
7	61464998	61464999	T	C	34	GENIC	homozygous	53931925
7	61465333	61465334	A	G	18	GENIC	homozygous	53931926
7	61465731	61465732	G	C	16	GENIC	homozygous	53931927
7	61465742	61465746	AAAT	----	14	GENIC	homozygous	53931928
7	61465827	61465828	T	C	27	GENIC	homozygous	53931929
7	61466024	61466025	G	C	29	GENIC	homozygous	53931930
7	61466521	61466522	C	T	17	GENIC	homozygous	53931931
7	61466827	61466828	A	ATGACTACAC	26	GENIC	homozygous	53931933
7	61458343	61458347	TGTG	----	11	GENIC	heterozygous	55355641
7	61458345	61458347	TG	--	11	GENIC	heterozygous	54978068