chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120526830	120526831	T	G	60	GENIC	homozygous	138197419
7	120527155	120527156	G	C	33	GENIC	homozygous	138197420
7	120527202	120527203	C	A	24	GENIC	heterozygous	403224321
7	120527212	120527213	C	T	23	GENIC	possibly homozygous	138197421
7	120527214	120527215	C	G	22	GENIC	possibly homozygous	138197422
7	120527217	120527218	C	T	22	GENIC	homozygous	138197423
7	120528563	120528564	C	A	62	GENIC	homozygous	138197424
7	120529597	120529598	C	A	49	GENIC	homozygous	138197425
7	120531623	120531624	A	G	60	GENIC	homozygous	138197426
7	120531965	120531966	T	C	62	GENIC	homozygous	138197427
7	120532653	120532654	A	G	67	GENIC	homozygous	138197428
7	120532897	120532898	C	T	66	GENIC	homozygous	138197429
7	120533039	120533040	A	G	63	GENIC	homozygous	138197430
7	120533072	120533073	A	G	59	GENIC	homozygous	138197431
7	120535577	120535578	G	A	61	GENIC	homozygous	147554927
7	120530237	120530238	A	T	33	GENIC	homozygous	147554925
7	120535134	120535135	G	A	55	GENIC	homozygous	147554926
7	120531807	120531808	G	C	48	GENIC	heterozygous	154479552
7	120531807	120531808	G	T	48	GENIC	possibly homozygous	154479553
7	120535587	120535588	T	C	57	GENIC	homozygous	138197432
7	120529569	120529570	T		32	GENIC	homozygous	137977957
7	120532675	120532675		AGGCCTGATTCAG	60	GENIC	homozygous	137977958