chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	81459238	81459239	A	G	31	GENIC	possibly homozygous	120779644
1	81459255	81459256	C	T	30	GENIC	possibly homozygous	120779645
1	81459783	81459784	A	C	35	GENIC	homozygous	120779646
1	81460860	81460861	A	G	31	GENIC	homozygous	108877027
1	81461571	81461572	G	T	24	GENIC	homozygous	120779647
1	81463520	81463521	C	T	23	GENIC	homozygous	120779648
1	81463743	81463744	C	T	23	GENIC	homozygous	120779649
1	81464847	81464848	C	T	47	GENIC	homozygous	120779650
1	81465135	81465136	A	T	21	GENIC	homozygous	120779651
1	81466159	81466160	G	A	32	GENIC	homozygous	108877072
1	81466234	81466235	T	C	30	GENIC	homozygous	120779652
1	81468276	81468276		G	30	GENIC	homozygous	131258734
1	81468724	81468725	C	T	24	GENIC	homozygous	120779653
1	81468890	81468891	A	G	34	GENIC	homozygous	120779654
1	81460883	81460887	ATTG		33	GENIC	homozygous	127398029
1	81464581	81464581		T	28	GENIC	homozygous	127398030
1	81464583	81464583		TG	28	GENIC	homozygous	127398031
1	81463096	81463097	C	T	35	GENIC	homozygous	134180103
1	81466629	81466630	A	G	17	GENIC	homozygous	134180104
1	81466455	81466456	T		22	GENIC	homozygous	134170529
1	81469601	81469601		AAGAAAGAAAGA	22	GENIC	homozygous	134170530
1	81471102	81471103	T	C	34	GENIC	homozygous	108877094