chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	44108945	44108946	G	-	10	GENIC	homozygous	47419566
17	44110512	44110513	G	A	21	GENIC	homozygous	47419568
17	44110885	44110886	G	A	32	GENIC	homozygous	47419570
17	44111602	44111603	T	C	19	GENIC	homozygous	47113744
17	44111709	44111710	A	C	19	GENIC	homozygous	47419572
17	44112183	44112184	T	A	18	GENIC	homozygous	47113746
17	44112589	44112593	AAAC	----	18	GENIC	homozygous	47113747
17	44112758	44112759	G	A	29	GENIC	homozygous	47419574
17	44112872	44112873	T	-	11	GENIC	homozygous	47419576
17	44112988	44112989	G	GCCCCCGTCA	28	GENIC	homozygous	47113748
17	44113598	44113599	T	TTC	17	GENIC	homozygous	47419578
17	44115301	44115303	AT	--	26	GENIC	homozygous	47709030
17	44115303	44115304	T	TCTCCA	25	GENIC	homozygous	47709032
17	44115621	44115622	C	T	18	GENIC	homozygous	47419580
17	44115684	44115685	T	-	8	GENIC	homozygous	47829064
17	44116511	44116512	G	C	27	GENIC	homozygous	47113762
17	44117297	44117298	C	G	16	GENIC	homozygous	47113763
17	44117522	44117523	G	GA	18	GENIC	homozygous	47113766
17	44118356	44118357	T	TACAC	8	GENIC	homozygous	47991015
17	44118711	44118712	A	C	30	GENIC	homozygous	47113773
17	44119191	44119192	T	A	23	GENIC	homozygous	47419588
17	44115889	44115890	G	A	22	GENIC	homozygous	47419582
17	44118169	44118170	G	C	19	GENIC	homozygous	47419584
17	44119053	44119054	A	-	13	GENIC	homozygous	47419586
17	44119481	44119482	T	C	27	GENIC	homozygous	47113777
17	44119684	44119685	C	T	36	GENIC	homozygous	47419590
17	44119792	44119793	T	A	25	GENIC	homozygous	47113779
17	44119908	44119909	C	CA	21	GENIC	homozygous	47113781
17	44120965	44120966	G	A	15	GENIC	homozygous	47419592
17	44120988	44120989	G	GA	15	GENIC	possibly homozygous	47113784
17	44121357	44121358	C	T	30	GENIC	homozygous	47113785