chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50410051	50410052	C	A	22	GENIC	homozygous	50471624
12	50410634	50410635	T	C	7	GENIC	homozygous	50238110
12	50410771	50410772	C	A	10	GENIC	possibly homozygous	50471625
12	50411462	50411463	A	C	21	GENIC	homozygous	50238116
12	50411687	50411688	G	T	13	GENIC	homozygous	50471626
12	50411690	50411691	G	T	13	GENIC	homozygous	50471627
12	50411991	50411992	A	C	29	GENIC	possibly homozygous	50471628
12	50412120	50412121	T	TCCCCACCCCCCATGCTTCTGGAGGTAGCACCTGAGACCTGATACTGTCCCCCACCCCCATGCTTCTGGAGGTAGCACCTGAGACCTGATACTG	22	GENIC	possibly homozygous	50624573
12	50412384	50412385	G	A	39	GENIC	homozygous	50238122
12	50412565	50412566	A	G	33	GENIC	homozygous	50471630
12	50413651	50413652	A	G	31	GENIC	homozygous	50238124
12	50414784	50414785	C	CAAAAAA	7	GENIC	heterozygous	50546908
12	50418061	50418062	A	G	23	GENIC	homozygous	50238154
12	50418457	50418458	T	C	29	GENIC	homozygous	50238162
12	50419050	50419051	T	TGCTA	2	GENIC	homozygous	50546909
12	50419078	50419079	A	AAG	4	GENIC	homozygous	50513900
12	50419079	50419080	C	CGCTCTACCACTGAGCTAAATCCCCAA	4	GENIC	homozygous	50513902
12	50419169	50419170	T	C	17	GENIC	homozygous	50238176
12	50420165	50420166	G	GCCCCC	7	GENIC	homozygous	50559421
12	50420858	50420859	C	CTGTG	11	GENIC	heterozygous	50604628
12	50421318	50421319	C	T	23	GENIC	homozygous	50471631
12	50421525	50421533	CCTTCCTC	--------	13	GENIC	homozygous	50624574
12	50421633	50421634	C	T	25	GENIC	possibly homozygous	50471632
12	50421764	50421765	T	C	19	GENIC	possibly homozygous	50238205
12	50421827	50421833	GTGTGC	------	19	GENIC	homozygous	50471633
12	50422629	50422630	T	C	26	GENIC	homozygous	50238219
12	50423691	50423692	T	TTGTGTGTG	19	GENIC	possibly homozygous	50624575
12	50424218	50424219	C	G	36	GENIC	homozygous	50471634
12	50425882	50425883	C	T	36	GENIC	homozygous	50471635
12	50426231	50426232	T	C	18	GENIC	homozygous	50238244
12	50427187	50427188	A	G	25	GENIC	homozygous	50238248
12	50427209	50427210	C	G	23	GENIC	homozygous	50471636
12	50427474	50427479	CTTTT	-----	11	GENIC	homozygous	50471637
12	50427490	50427491	C	CT	12	GENIC	homozygous	50344018
12	50427506	50427507	T	-	15	GENIC	homozygous	50471638
12	50428146	50428149	CTG	---	31	GENIC	possibly homozygous	50471639
12	50428415	50428416	G	-	23	GENIC	homozygous	50471640
12	50428676	50428677	G	A	16	GENIC	possibly homozygous	50471641
12	50429597	50429598	G	A	13	GENIC	homozygous	50624576
12	50429601	50429602	G	A	14	GENIC	homozygous	50624577
12	50429983	50429984	G	A	22	GENIC	homozygous	50471642
12	50430226	50430227	T	TA	8	GENIC	homozygous	50471643
12	50430501	50430502	G	T	16	GENIC	homozygous	50238273
12	50430513	50430514	A	AAAAC	16	GENIC	homozygous	50238275
12	50431086	50431087	C	T	48	GENIC	homozygous	50238279
12	50431258	50431259	T	C	37	GENIC	homozygous	50471644
12	50431440	50431441	A	C	22	GENIC	possibly homozygous	50238285
12	50431736	50431737	A	G	21	GENIC	homozygous	50238287
12	50433543	50433544	T	C	16	GENIC	homozygous	50238296
12	50434001	50434002	T	C	28	GENIC	homozygous	50238298
12	50434108	50434109	G	A	33	GENIC	homozygous	50238300
12	50434151	50434152	A	G	29	GENIC	homozygous	50238302
12	50434287	50434288	T	C	40	GENIC	homozygous	50238304
12	50434850	50434851	C	T	34	GENIC	homozygous	50238306
12	50436001	50436002	C	CAG	21	GENIC	homozygous	50238310
12	50436967	50436968	T	C	32	GENIC	possibly homozygous	50238314