chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	27038485	27038486	C	A	29	GENIC	homozygous	50373978
12	27038740	27038741	G	A	21	GENIC	homozygous	50467379
12	27038788	27038789	G	T	22	GENIC	homozygous	50373982
12	27038817	27038818	T	C	33	GENIC	homozygous	50419802
12	27038830	27038831	C	T	30	GENIC	homozygous	50373984
12	27039622	27039623	C	T	16	GENIC	homozygous	50151594
12	27040382	27040384	TT	--	8	GENIC	possibly homozygous	50151598
12	27040383	27040384	T	-	8	GENIC	heterozygous	50373986
12	27041027	27041028	A	G	25	GENIC	possibly homozygous	50151600
12	27041970	27041971	A	ATT	8	GENIC	possibly homozygous	50151604
12	27042173	27042174	A	AT	5	GENIC	heterozygous	50151606
12	27042174	27042175	T	TTG	7	GENIC	heterozygous	50151608
12	27043742	27043743	T	C	22	GENIC	homozygous	50151617
12	27043823	27043824	G	GTCTC	13	GENIC	heterozygous	50569642
12	27043831	27043832	C	CTG	13	GENIC	heterozygous	50374004
12	27043877	27043878	C	CTGTG	12	GENIC	possibly homozygous	50440445
12	27043904	27043905	C	CGT	24	GENIC	possibly homozygous	50405783
12	27044701	27044702	A	G	21	GENIC	homozygous	50151627
12	27044784	27044785	A	G	24	GENIC	homozygous	50151629
12	27045115	27045116	G	A	19	GENIC	homozygous	50467381
12	27045775	27045776	A	G	17	GENIC	homozygous	50151631
12	27046305	27046306	C	T	19	GENIC	homozygous	50467383
12	27046816	27046817	G	-	12	GENIC	homozygous	50467385
12	27048900	27048901	T	C	20	GENIC	homozygous	50301162
12	27048930	27048931	A	AG	22	GENIC	homozygous	50151651
12	27049036	27049037	G	T	16	GENIC	homozygous	50151653
12	27049114	27049115	C	CTCGTGAGCGAG	10	GENIC	homozygous	50151655
12	27049147	27049148	A	G	9	GENIC	homozygous	50151659
12	27050113	27050114	G	A	20	GENIC	homozygous	50419806
12	27050629	27050630	C	-	18	GENIC	homozygous	50151663
12	27050892	27050893	C	CA	26	GENIC	homozygous	50151665
12	27050893	27050894	G	GGCTGTGCATGGAAAAA	25	GENIC	homozygous	50151667
12	27051108	27051109	C	T	16	GENIC	homozygous	50467391
12	27051118	27051119	G	C	13	GENIC	homozygous	50419807
12	27051432	27051433	C	T	25	GENIC	homozygous	50419809
12	27051865	27051866	G	A	28	GENIC	homozygous	50405795
12	27052249	27052250	C	T	27	GENIC	homozygous	50419810
12	27052370	27052371	A	-	12	GENIC	heterozygous	50405797
12	27052385	27052386	A	G	24	GENIC	possibly homozygous	50539515
12	27052710	27052711	C	CTATG	14	GENIC	possibly homozygous	50151683
12	27053853	27054058	GGCGTGGCTCAGTGGTAGAGCCCCTGCCTAGAATCCCCCAGGGAGGGGCGTGGCTCAGTGGTAGAGCCCCTGCCTAGAATCCCCCAGTGAGGGGCTGGGGGTGTGGCTCAGTGGTAGAGCACCTGCCTAGAATCCCCCAGTGAGGGGCTGGGGGCGTGGCTCAGTGGTAGAGCCCCTGCCTAGAATCCCCCAGTGAGGGGCTGGG	-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------	12	GENIC	heterozygous	50509512
12	27054718	27054719	C	A	10	GENIC	homozygous	50467397
12	27056007	27056012	AAAAA	-----	4	GENIC	heterozygous	50600637
12	27056008	27056012	AAAA	----	4	GENIC	heterozygous	50539516
12	27057298	27057299	A	G	15	GENIC	homozygous	50151743
12	27059525	27059526	T	C	17	GENIC	homozygous	50151767
12	27060059	27060063	CTTA	----	7	GENIC	possibly homozygous	50539517
12	27060094	27060102	CCTCCCTT	--------	15	GENIC	possibly homozygous	50539518
12	27061975	27061981	GTTGTC	------	27	GENIC	homozygous	50151793
12	27062003	27062004	G	A	28	GENIC	homozygous	50467401
12	27062607	27062608	G	A	16	GENIC	homozygous	50467403
12	27065029	27065030	T	TCA	3	GENIC	heterozygous	50374044
12	27065801	27065802	G	A	13	GENIC	homozygous	50151837
12	27065846	27065847	G	C	14	GENIC	homozygous	50151839
12	27065870	27065872	CC	--	10	GENIC	heterozygous	50151841
12	27065871	27065872	C	-	10	GENIC	possibly homozygous	50374051
12	27066213	27066214	C	A	20	GENIC	possibly homozygous	50151843
12	27066888	27066889	C	T	18	GENIC	homozygous	50151847
12	27067294	27067295	T	-	12	GENIC	heterozygous	50151849
12	27070682	27070683	T	TG	5	GENIC	homozygous	50151885