chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120526830	120526831	T	G	30	GENIC	homozygous	138197419
7	120527155	120527156	G	C	9	GENIC	homozygous	138197420
7	120527202	120527203	C	A	9	GENIC	heterozygous	403224321
7	120527212	120527213	C	T	9	GENIC	possibly homozygous	138197421
7	120527214	120527215	C	G	9	GENIC	possibly homozygous	138197422
7	120527217	120527218	C	T	6	GENIC	homozygous	138197423
7	120528563	120528564	C	A	13	GENIC	homozygous	138197424
7	120529569	120529570	T		17	GENIC	homozygous	137977957
7	120529597	120529598	C	A	18	GENIC	homozygous	138197425
7	120531623	120531624	A	G	23	GENIC	homozygous	138197426
7	120531965	120531966	T	C	18	GENIC	homozygous	138197427
7	120532653	120532654	A	G	26	GENIC	homozygous	138197428
7	120532675	120532675		AGGCCTGATTCAG	23	GENIC	homozygous	137977958
7	120532897	120532898	C	T	23	GENIC	homozygous	138197429
7	120533039	120533040	A	G	16	GENIC	homozygous	138197430
7	120533072	120533073	A	G	14	GENIC	homozygous	138197431
7	120535587	120535588	T	C	15	GENIC	homozygous	138197432
7	120535959	120535960	G	A	22	GENIC	homozygous	138197433
7	120531807	120531808	G	C	9	GENIC	homozygous	154479552
7	120531807	120531808	G	T	9	GENIC	heterozygous	154479553