chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	27161601	27161602	T	C	22	GENIC	homozygous	50152746
12	27161840	27161841	G	A	32	GENIC	homozygous	50406003
12	27162644	27162645	G	A	32	GENIC	homozygous	50406005
12	27164184	27164185	T	TCTCTCTCC	10	GENIC	possibly homozygous	50539564
12	27164196	27164197	G	C	15	GENIC	homozygous	50152768
12	27164288	27164289	T	C	14	GENIC	homozygous	50152772
12	27164857	27164858	G	GA	21	GENIC	homozygous	50152776
12	27165458	27165459	A	G	36	GENIC	homozygous	50152778
12	27165881	27165882	G	C	29	GENIC	homozygous	50152784
12	27165954	27165955	C	T	24	GENIC	homozygous	50406007
12	27167059	27167060	A	G	21	GENIC	homozygous	50152786
12	27167382	27167383	T	C	23	GENIC	homozygous	50152788
12	27167706	27167707	G	A	34	GENIC	homozygous	50406009
12	27168084	27168085	A	G	22	GENIC	homozygous	50152790
12	27168314	27168315	T	-	15	GENIC	homozygous	50152794
12	27168381	27168382	A	G	11	GENIC	homozygous	50152796
12	27164858	27164859	C	T	22	GENIC	homozygous	50509554