chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	142116946	142116947	A	G	36	GENIC	homozygous	115941391
7	142116993	142116994	T	G	44	GENIC	homozygous	116097462
7	142117902	142117903	T	C	37	GENIC	heterozygous	116097464
7	142117906	142117907	T	C	32	GENIC	heterozygous	116097466
7	142117994	142117995	C	T	19	GENIC	possibly homozygous	116097468
7	142118004	142118005	C	T	20	GENIC	possibly homozygous	116097470
7	142118009	142118010	G	A	20	GENIC	possibly homozygous	116097472
7	142118010	142118011	C	T	20	GENIC	possibly homozygous	116097474
7	142118014	142118015	T	C	23	GENIC	possibly homozygous	116097476
7	142118020	142118021	C	T	32	GENIC	possibly homozygous	116097478
7	142119389	142119390	A	G	54	GENIC	homozygous	115941394
7	142119769	142119770	C	G	55	GENIC	possibly homozygous	115941396
7	142120178	142120179	G	A	42	GENIC	homozygous	115941397
7	142120934	142120935	C	T	38	GENIC	homozygous	115941398
7	142121712	142121713	A	G	47	GENIC	homozygous	115941400
7	142124053	142124054	C	T	38	GENIC	homozygous	116097480
7	142124979	142124980	A	G	45	GENIC	homozygous	115941403
7	142125765	142125766	A	T	45	GENIC	homozygous	116097482
7	142126083	142126084	G	A	47	GENIC	possibly homozygous	116097484
7	142126337	142126338	T	C	51	GENIC	homozygous	116097486
7	142126453	142126454	G	C	47	GENIC	homozygous	116097488
7	142126700	142126701	C	G	49	GENIC	homozygous	116097490
7	142127934	142127935	G	A	13	GENIC	homozygous	116097492
7	142127945	142127946	G	C	11	GENIC	homozygous	116097494
7	142127973	142127974	C	A	7	GENIC	homozygous	115941406
7	142128052	142128053	C	T	18	GENIC	homozygous	116097496
7	142128546	142128547	G	A	39	GENIC	homozygous	116097498
7	142128950	142128951	C	T	42	GENIC	homozygous	116097500
7	142131414	142131415	C	T	36	GENIC	homozygous	116097502
7	142132137	142132138	A	T	33	GENIC	possibly homozygous	116097504