chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	27161594	27161595	C	A	36	GENIC	homozygous	50152744
12	27161601	27161602	T	C	34	GENIC	homozygous	50152746
12	27161861	27161862	C	T	24	GENIC	homozygous	50152748
12	27161961	27161962	A	G	37	GENIC	homozygous	50152750
12	27162073	27162074	T	C	66	GENIC	homozygous	50152752
12	27162647	27162648	C	T	48	GENIC	homozygous	50152754
12	27163156	27163157	C	T	33	GENIC	homozygous	50152756
12	27163261	27163262	A	C	39	GENIC	homozygous	50152758
12	27163452	27163456	TCTA	----	37	GENIC	homozygous	50152760
12	27163726	27163727	T	-	43	GENIC	homozygous	50152762
12	27163728	27163729	C	A	42	GENIC	homozygous	50611503
12	27164065	27164066	C	T	23	GENIC	homozygous	50152764
12	27164066	27164067	C	T	23	GENIC	homozygous	50152766
12	27164148	27164149	A	ACTCTCT	8	GENIC	heterozygous	50614817
12	27164196	27164197	G	C	9	GENIC	homozygous	50152768
12	27164211	27164212	C	T	4	GENIC	homozygous	50152770
12	27164288	27164289	T	C	20	GENIC	homozygous	50152772
12	27164350	27164351	G	A	33	GENIC	homozygous	50152774
12	27164857	27164858	G	GA	31	GENIC	homozygous	50152776
12	27164858	27164859	C	T	31	GENIC	homozygous	50509554
12	27165068	27165069	A	AG	3	GENIC	homozygous	50614818
12	27165458	27165459	A	G	42	GENIC	homozygous	50152778
12	27165521	27165522	C	T	30	GENIC	homozygous	50152780
12	27165577	27165578	C	T	46	GENIC	homozygous	50152782
12	27165881	27165882	G	C	69	GENIC	homozygous	50152784
12	27167059	27167060	A	G	34	GENIC	homozygous	50152786
12	27167382	27167383	T	C	46	GENIC	homozygous	50152788
12	27168084	27168085	A	G	51	GENIC	homozygous	50152790
12	27168314	27168315	T	-	34	GENIC	homozygous	50152794
12	27168381	27168382	A	G	42	GENIC	possibly homozygous	50152796