chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12610888	12610889	T	C	31	GENIC	homozygous	53791320
7	12613887	12613890	CCT	---	21	GENIC	homozygous	53791322
7	12614495	12614496	A	C	19	GENIC	homozygous	53791323
7	12618900	12618901	C	A	30	GENIC	homozygous	53791325
7	12618999	12619000	G	A	36	GENIC	homozygous	53791326
7	12619481	12619482	G	GA	16	GENIC	possibly homozygous	54885005
7	12619684	12619685	G	A	28	GENIC	homozygous	53791328
7	12621137	12621138	A	AACACACAC	2	GENIC	homozygous	55071106
7	12622061	12622062	G	A	32	GENIC	homozygous	53791330
7	12622112	12622113	G	A	24	GENIC	homozygous	53791331
7	12622113	12622114	G	A	24	GENIC	homozygous	53791332
7	12622137	12622138	C	CAAAA	16	GENIC	homozygous	55057502
7	12622383	12622384	A	G	28	GENIC	possibly homozygous	53791335
7	12622659	12622660	A	G	33	GENIC	homozygous	53791336
7	12624322	12624323	C	G	33	GENIC	homozygous	53791338
7	12624403	12624404	T	TAG	17	GENIC	homozygous	53791340
7	12624596	12624597	G	A	37	GENIC	homozygous	54630467
7	12624768	12624769	C	T	19	GENIC	homozygous	53791341
7	12625247	12625248	C	T	24	GENIC	homozygous	53791342
7	12625312	12625314	AG	--	24	GENIC	heterozygous	54630469
7	12625357	12625358	C	G	35	GENIC	possibly homozygous	53791344
7	12625553	12625554	G	GGAA	2	GENIC	heterozygous	56142397
7	12625575	12625576	G	GA	19	GENIC	homozygous	56142400
7	12625576	12625577	T	TGG	2	GENIC	heterozygous	56142403
7	12625762	12625763	T	TA	8	GENIC	possibly homozygous	55920282
7	12626275	12626278	GTC	---	22	GENIC	homozygous	54630477
7	12626903	12626904	G	-	19	GENIC	homozygous	54630479