chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	66334457	66334458	T	C	22	GENIC	heterozygous	59708703
2	66334458	66334459	G	A	22	GENIC	heterozygous	59708705
2	66334749	66334755	CTGGAC	------	5	GENIC	heterozygous	59708707
2	66334769	66334770	A	G	11	GENIC	possibly homozygous	58858165
2	66334805	66334806	C	A	18	GENIC	homozygous	59708709
2	66334906	66334907	C	A	26	GENIC	homozygous	59708711
2	66335133	66335134	A	T	6	GENIC	homozygous	60444607
2	66335136	66335137	C	A	8	GENIC	homozygous	60444608
2	66335137	66335138	C	G	9	GENIC	homozygous	60113633
2	66335141	66335142	G	A	9	GENIC	homozygous	59708713
2	66335197	66335198	A	G	13	GENIC	homozygous	59708715
2	66335266	66335267	A	T	5	GENIC	homozygous	59708717
2	66335275	66335276	G	GCACACACACACACACACACACACACACACACACACA	2	GENIC	homozygous	60482851
2	66335278	66335279	T	C	1	GENIC	homozygous	60482852
2	66335280	66335281	T	C	1	GENIC	homozygous	60482853
2	66335347	66335348	T	C	9	GENIC	heterozygous	59708719
2	66335348	66335349	A	G	8	GENIC	heterozygous	59708721
2	66335421	66335422	T	C	12	GENIC	possibly homozygous	59708723
2	66335532	66335534	TT	--	14	GENIC	possibly homozygous	59708725
2	66335708	66335709	C	T	23	GENIC	possibly homozygous	58858174
2	66335861	66335862	T	C	15	GENIC	possibly homozygous	59708727
2	66336025	66336026	G	C	23	GENIC	homozygous	59708729
2	66336132	66336133	G	A	9	GENIC	homozygous	59708731
2	66336234	66336235	A	G	21	GENIC	homozygous	59708733
2	66336310	66336311	A	G	22	GENIC	possibly homozygous	59708735
2	66336499	66336500	G	A	15	GENIC	possibly homozygous	59708737
2	66336763	66336764	G	A	20	GENIC	homozygous	59708739
2	66336893	66336894	C	A	17	GENIC	possibly homozygous	59708741
2	66336975	66336976	T	C	28	GENIC	possibly homozygous	59708743
2	66337214	66337215	G	C	16	GENIC	possibly homozygous	59708745
2	66337258	66337259	G	A	14	GENIC	possibly homozygous	59708747
2	66337889	66337890	C	T	22	GENIC	homozygous	59708749
2	66338127	66338128	C	T	3	GENIC	homozygous	59708751