chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	71510884	71510885	C	A	21	GENIC	homozygous	47180662
17	71511332	71511333	G	A	18	GENIC	homozygous	47180663
17	71512074	71512075	G	A	17	GENIC	homozygous	47180664
17	71512698	71512699	T	C	17	GENIC	homozygous	47180665
17	71512750	71512751	A	G	13	GENIC	homozygous	47180666
17	71514504	71514505	A	G	20	GENIC	homozygous	47180667
17	71514571	71514577	AGAGAG	------	4	GENIC	heterozygous	47752186
17	71514841	71514842	T	C	24	GENIC	homozygous	47180668
17	71515577	71515578	A	T	28	GENIC	homozygous	47180669
17	71515980	71515982	AA	--	10	GENIC	homozygous	47180670
17	71520315	71520316	A	G	22	GENIC	homozygous	47180673
17	71520480	71520481	G	T	25	GENIC	homozygous	47180674
17	71521226	71521227	T	TTTTTTTGGTTC	6	GENIC	homozygous	47180675
17	71521866	71521867	T	TGTGTGAGA	9	GENIC	possibly homozygous	47752188
17	71522482	71522483	C	T	25	GENIC	homozygous	47180676
17	71523095	71523099	CACA	----	11	GENIC	homozygous	47752190
17	71523176	71523184	ACACACAC	--------	5	GENIC	homozygous	47752192
17	71525062	71525063	G	A	27	GENIC	homozygous	47180678
17	71526162	71526163	A	G	22	GENIC	homozygous	47180679
17	71527297	71527298	C	CTG	4	GENIC	homozygous	47752196
17	71527655	71527656	G	-	16	GENIC	homozygous	47180681
17	71527753	71527755	AA	--	19	GENIC	homozygous	47180682
17	71528830	71528831	T	TTGTG	6	GENIC	homozygous	47180683
17	71529046	71529047	C	CT	21	GENIC	homozygous	47180684
17	71529463	71529464	T	C	16	GENIC	homozygous	47180685
17	71516940	71516941	C	CTGTG	7	GENIC	heterozygous	47794031