chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	57029294	57029294		CTTGCTAGGCAAGCGCTCT	6	GENIC	homozygous	129460707
17	57029297	57029297		A	7	GENIC	homozygous	129460708
17	57029301	57029301		GCTAAATC	7	GENIC	homozygous	129460709
17	57029305	57029306	C	A	8	GENIC	homozygous	119346131
17	57050069	57050069		GA	35	GENIC	homozygous	129460721
17	57052437	57052438	G		10	GENIC	heterozygous	130600297
17	57052558	57052559	T		14	GENIC	homozygous	129460724
17	57052597	57052598	A		14	GENIC	homozygous	129460725
17	57052621	57052628	CCATCCT		14	GENIC	homozygous	129460726
17	57052640	57052641	C		16	GENIC	homozygous	129460727
17	57052661	57052662	T		20	GENIC	homozygous	129460728
17	57052773	57052774	G		35	GENIC	homozygous	129460729
17	57053004	57053005	C		6	GENIC	homozygous	129460730
17	57053010	57053010		A	6	GENIC	homozygous	129460731
17	57053010	57053011	C	A	4	GENIC	homozygous	129498851
17	57053164	57053164		C	10	GENIC	homozygous	129460732
17	57053301	57053301		T	6	GENIC	homozygous	129460733
17	57053342	57053343	C		4	GENIC	homozygous	129460734
17	57058506	57058506		ATCC	20	GENIC	possibly homozygous	130464147
17	57052388	57052392	AGTT		11	GENIC	homozygous	130464142
17	57052409	57052409		T	12	GENIC	homozygous	130464143
17	57052426	57052428	CC		13	GENIC	homozygous	130464144
17	57052431	57052432	T		13	GENIC	homozygous	130464145
17	57052462	57052465	CAC		14	GENIC	heterozygous	130464146
17	57052409	57052410	G	A	12	GENIC	homozygous	130468986
17	57068332	57068333	A	C	37	GENIC	homozygous	111068281
17	57068342	57068342		T	38	GENIC	homozygous	129460741
17	57068478	57068478		G	15	GENIC	homozygous	129460742
17	57068508	57068508		GG	12	GENIC	homozygous	129460743
17	57068523	57068524	G		11	GENIC	homozygous	129460744
17	57068533	57068533		G	11	GENIC	homozygous	129460745
17	57068536	57068536		A	11	GENIC	homozygous	129460746
17	57076904	57076905	G	T	17	GENIC	heterozygous	132509174