chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12610888	12610889	T	C	7	GENIC	homozygous	53791320
7	12613887	12613890	CCT	---	1	GENIC	homozygous	53791322
7	12614347	12614348	A	-	7	GENIC	heterozygous	54711695
7	12614495	12614496	A	C	18	GENIC	homozygous	53791323
7	12614537	12614538	C	T	5	GENIC	heterozygous	53791324
7	12618900	12618901	C	A	23	GENIC	homozygous	53791325
7	12618999	12619000	G	A	13	GENIC	possibly homozygous	53791326
7	12619188	12619189	G	A	20	GENIC	heterozygous	53791327
7	12619684	12619685	G	A	29	GENIC	possibly homozygous	53791328
7	12622061	12622062	G	A	5	GENIC	homozygous	53791330
7	12622383	12622384	A	G	14	GENIC	possibly homozygous	53791335
7	12622659	12622660	A	G	9	GENIC	homozygous	53791336
7	12624229	12624230	T	TA	3	GENIC	heterozygous	53791337
7	12624768	12624769	C	T	7	GENIC	homozygous	53791341
7	12625247	12625248	C	T	12	GENIC	homozygous	53791342
7	12625260	12625261	G	C	15	GENIC	possibly homozygous	53791343
7	12625357	12625358	C	G	11	GENIC	possibly homozygous	53791344
7	12625409	12625410	C	T	9	GENIC	heterozygous	53791345
7	12625762	12625763	T	TA	2	GENIC	heterozygous	55920282
7	12625920	12625921	C	A	1	GENIC	homozygous	53791355
7	12625928	12625929	G	A	1	GENIC	homozygous	53791356
7	12626271	12626272	C	T	2	GENIC	homozygous	53791358
7	12627468	12627469	T	C	2	GENIC	homozygous	53791361