chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	142116946	142116947	A	G	40	GENIC	homozygous	115941391
7	142117992	142117993	C	T	17	GENIC	possibly homozygous	115941392
7	142118006	142118007	C	T	22	GENIC	heterozygous	115941393
7	142119389	142119390	A	G	31	GENIC	homozygous	115941394
7	142119473	142119474	C	T	26	GENIC	heterozygous	115941395
7	142119769	142119770	C	G	38	GENIC	homozygous	115941396
7	142120178	142120179	G	A	55	GENIC	homozygous	115941397
7	142120934	142120935	C	T	49	GENIC	homozygous	115941398
7	142121603	142121604	G	A	36	GENIC	possibly homozygous	115941399
7	142121712	142121713	A	G	37	GENIC	homozygous	115941400
7	142122329	142122330	G	T	34	GENIC	possibly homozygous	115941401
7	142124567	142124568	C	T	44	GENIC	homozygous	115941402
7	142124979	142124980	A	G	53	GENIC	homozygous	115941403
7	142125656	142125657	C	T	63	GENIC	possibly homozygous	115941404
7	142127176	142127177	C	T	56	GENIC	homozygous	115941405
7	142127973	142127974	C	A	15	GENIC	heterozygous	115941406
7	142128672	142128673	G	A	50	GENIC	homozygous	115941407
7	142128972	142128973	A	G	33	GENIC	homozygous	115941408