chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	142116946	142116947	A	G	16	GENIC	homozygous	115941391
7	142116993	142116994	T	G	16	GENIC	homozygous	116097462
7	142117447	142117448	C	A	12	GENIC	homozygous	116233190
7	142119389	142119390	A	G	14	GENIC	homozygous	115941394
7	142119769	142119770	C	G	17	GENIC	homozygous	115941396
7	142120178	142120179	G	A	35	GENIC	homozygous	115941397
7	142120934	142120935	C	T	12	GENIC	homozygous	115941398
7	142121712	142121713	A	G	21	GENIC	homozygous	115941400
7	142124053	142124054	C	T	19	GENIC	homozygous	116097480
7	142124979	142124980	A	G	29	GENIC	homozygous	115941403
7	142125765	142125766	A	T	22	GENIC	homozygous	116097482
7	142126083	142126084	G	A	22	GENIC	homozygous	116097484
7	142126337	142126338	T	C	16	GENIC	homozygous	116097486
7	142126453	142126454	G	C	20	GENIC	homozygous	116097488
7	142126700	142126701	C	G	12	GENIC	homozygous	116097490
7	142128052	142128053	C	T	10	GENIC	homozygous	116097496
7	142128546	142128547	G	A	15	GENIC	homozygous	116097498
7	142128950	142128951	C	T	15	GENIC	homozygous	116097500
7	142131414	142131415	C	T	9	GENIC	homozygous	116097502
7	142132137	142132138	A	T	12	GENIC	homozygous	116097504