chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12610888	12610889	T	C	26	GENIC	homozygous	53791320
7	12611549	12611550	C	T	29	GENIC	possibly homozygous	54711693
7	12613887	12613890	CCT	---	31	GENIC	homozygous	53791322
7	12614347	12614348	A	-	26	GENIC	homozygous	54711695
7	12614403	12614404	G	A	37	GENIC	homozygous	54711697
7	12618900	12618901	C	A	42	GENIC	homozygous	53791325
7	12619684	12619685	G	A	34	GENIC	homozygous	53791328
7	12622061	12622062	G	A	34	GENIC	homozygous	53791330
7	12622147	12622148	A	AAAAT	25	GENIC	homozygous	54181792
7	12622659	12622660	A	G	35	GENIC	homozygous	53791336
7	12623522	12623523	T	C	29	GENIC	homozygous	54711699
7	12624322	12624323	C	G	32	GENIC	homozygous	53791338
7	12624403	12624404	T	TAG	22	GENIC	homozygous	53791340
7	12624462	12624463	A	G	33	GENIC	homozygous	54711701
7	12624596	12624597	G	A	40	GENIC	homozygous	54630467
7	12624768	12624769	C	T	42	GENIC	homozygous	53791341
7	12625551	12625552	C	CG	11	GENIC	homozygous	54711703
7	12625577	12625578	C	T	20	GENIC	homozygous	53791347
7	12625587	12625588	A	G	19	GENIC	possibly homozygous	54711705
7	12625661	12625662	A	G	17	GENIC	homozygous	53791351
7	12625672	12625673	C	T	15	GENIC	homozygous	53791352
7	12625714	12625715	C	T	15	GENIC	homozygous	54711707
7	12625762	12625763	T	TAAA	11	GENIC	homozygous	54181793
7	12625801	12625802	C	CG	14	GENIC	heterozygous	53791354
7	12625801	12625802	C	G	28	GENIC	possibly homozygous	54630473
7	12625973	12625974	G	A	24	GENIC	homozygous	54630475
7	12626275	12626278	GTC	---	28	GENIC	homozygous	54630477
7	12626903	12626904	G	-	22	GENIC	homozygous	54630479
7	12626913	12626914	G	GA	22	GENIC	homozygous	53791359