chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	166031252	166031272	GCCTTGCGCTCGCTAGGCAA		41	GENIC	homozygous	127453278
1	166031601	166031602	C	T	28	GENIC	homozygous	108355978
1	166031632	166031633	C	T	27	GENIC	homozygous	108355979
1	166031659	166031660	A	G	30	GENIC	homozygous	108355980
1	166032837	166032838	T	G	37	GENIC	homozygous	108355981
1	166033099	166033099		CAT	36	GENIC	possibly homozygous	127453279
1	166033538	166033539	C	T	47	GENIC	homozygous	108355982
1	166033544	166033545	C		49	GENIC	homozygous	127453280
1	166033956	166033957	T	C	51	GENIC	homozygous	108355983
1	166034463	166034464	A	G	46	GENIC	homozygous	108355984
1	166034474	166034475	G	A	45	GENIC	homozygous	108355985
1	166034506	166034507	C		44	GENIC	homozygous	127453281
1	166034841	166034842	G	A	46	GENIC	homozygous	108355986
1	166035030	166035031	A		26	GENIC	homozygous	127453282
1	166035059	166035059		T	16	GENIC	homozygous	127453283
1	166036771	166036772	T	C	35	GENIC	possibly homozygous	108355987
1	166038099	166038100	T	C	48	GENIC	homozygous	108355988
1	166038102	166038103	A	G	48	GENIC	homozygous	108355989
1	166038566	166038567	C	T	37	GENIC	homozygous	108355990
1	166039394	166039395	T	C	43	GENIC	homozygous	108355991
1	166040885	166040886	A	G	31	GENIC	homozygous	108355992
1	166041051	166041051		GTGTGTGTGA	47	GENIC	homozygous	127453284
1	166041095	166041096	A	G	43	GENIC	homozygous	108355994
1	166041868	166041869	C	T	41	GENIC	homozygous	108355996
1	166043101	166043101		CTCT	39	GENIC	homozygous	127453285
1	166043441	166043442	G	A	40	GENIC	homozygous	108355997
1	166043557	166043557		CACCCAAA	34	GENIC	homozygous	127453286
1	166043558	166043558		GCA	36	GENIC	homozygous	127453287
1	166043950	166043951	A	G	37	GENIC	homozygous	108355998
1	166044740	166044740		TT	35	GENIC	homozygous	127453288
1	166044972	166044973	G	A	37	GENIC	homozygous	108355999
1	166038508	166038509	C	T	27	GENIC	heterozygous	108751544
1	166038510	166038511	C	T	27	GENIC	heterozygous	127562538