chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	122603571	122603572	G	A	40	GENIC	homozygous	115860969
7	122604230	122604231	G	T	58	GENIC	homozygous	115860971
7	122604231	122604232	A	T	59	GENIC	homozygous	115860973
7	122604569	122604570	C	A	17	GENIC	homozygous	115860975
7	122608102	122608103	G	A	47	GENIC	homozygous	115860977
7	122608157	122608158	T	A	31	GENIC	homozygous	115860979
7	122609735	122609736	T	C	41	GENIC	homozygous	115860983
7	122609835	122609836	A	G	24	GENIC	homozygous	115860985
7	122610611	122610612	G	A	22	GENIC	homozygous	115860987
7	122611371	122611372	A	C	19	GENIC	homozygous	115860989
7	122614783	122614784	C	T	19	GENIC	homozygous	115860991
7	122616079	122616080	T	A	25	GENIC	homozygous	115860993
7	122616678	122616679	A	C	28	GENIC	homozygous	115860995
7	122618006	122618007	T	G	26	GENIC	homozygous	115860997
7	122621427	122621428	G	A	23	GENIC	homozygous	118259232
7	122623363	122623364	A	G	21	GENIC	homozygous	115860999
7	122624013	122624014	A	G	35	GENIC	possibly homozygous	115861003
7	122624872	122624873	C	A	20	GENIC	homozygous	118286390
7	122627282	122627283	C	T	28	GENIC	homozygous	115861005
7	122627284	122627285	C	T	28	GENIC	homozygous	115861007
7	122628870	122628871	G	T	23	GENIC	homozygous	116226298
7	122629068	122629069	A	T	29	GENIC	homozygous	115861013
7	122629071	122629072	G	A	28	GENIC	homozygous	115861015
7	122630844	122630845	T	C	27	GENIC	homozygous	115861019
7	122631057	122631058	A	G	38	GENIC	homozygous	115861023
7	122632986	122632987	G	T	22	GENIC	homozygous	115861029
7	122633265	122633266	C	A	36	GENIC	homozygous	115861031