chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	44108944	44108945	A	AG	14	GENIC	homozygous	47113741
17	44109072	44109073	C	T	17	GENIC	homozygous	47113742
17	44111602	44111603	T	C	28	GENIC	homozygous	47113744
17	44112183	44112184	T	A	24	GENIC	homozygous	47113746
17	44112589	44112593	AAAC	----	22	GENIC	homozygous	47113747
17	44112988	44112989	G	GCCCCCGTCA	32	GENIC	homozygous	47113748
17	44113437	44113438	G	T	23	GENIC	homozygous	47113750
17	44113585	44113586	C	T	14	GENIC	homozygous	47113752
17	44113591	44113592	C	CTTTTTTT	9	GENIC	heterozygous	47709028
17	44113592	44113594	TT	--	9	GENIC	heterozygous	47113753
17	44115301	44115303	AT	--	25	GENIC	homozygous	47709030
17	44115303	44115304	T	TCTCCA	23	GENIC	homozygous	47709032
17	44115683	44115685	TT	--	5	GENIC	homozygous	47709034
17	44116511	44116512	G	C	22	GENIC	homozygous	47113762
17	44117297	44117298	C	G	23	GENIC	homozygous	47113763
17	44117433	44117434	T	G	16	GENIC	homozygous	47113765
17	44117522	44117523	G	GA	19	GENIC	homozygous	47113766
17	44117976	44117980	AAAC	----	24	GENIC	homozygous	47113768
17	44118390	44118404	CACACACACACACG	--------------	22	GENIC	possibly homozygous	47113769
17	44118550	44118551	C	T	34	GENIC	homozygous	47113771
17	44118711	44118712	A	C	29	GENIC	homozygous	47113773
17	44119029	44119041	CCCAGATGCCAT	------------	23	GENIC	homozygous	47113774
17	44119261	44119262	A	G	32	GENIC	homozygous	47113776
17	44119481	44119482	T	C	32	GENIC	homozygous	47113777
17	44119792	44119793	T	A	34	GENIC	homozygous	47113779
17	44119908	44119909	C	CA	30	GENIC	homozygous	47113781
17	44120426	44120429	ATG	---	30	GENIC	homozygous	47113782
17	44120988	44120989	G	GA	21	GENIC	possibly homozygous	47113784
17	44120988	44120989	G	GAA	21	GENIC	heterozygous	47739436
17	44121357	44121358	C	T	25	GENIC	homozygous	47113785