chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	29940338	29940339	T	C	53	GENIC	homozygous	138049624
7	29941986	29941987	G	A	51	GENIC	homozygous	138049625
7	29943431	29943432	A	C	65	GENIC	homozygous	138049626
7	29943522	29943523	G	C	48	GENIC	homozygous	138049627
7	29945167	29945168	A	G	74	GENIC	homozygous	138049628
7	29945403	29945404	G	T	49	GENIC	homozygous	138049629
7	29945673	29945674	T	C	57	GENIC	homozygous	138049630
7	29945717	29945718	T	A	63	GENIC	homozygous	138049631
7	29946195	29946196	A	G	40	GENIC	homozygous	138049632
7	29947930	29947931	T	C	44	GENIC	homozygous	138049633
7	29949007	29949008	T	A	43	GENIC	homozygous	138049634
7	29940984	29940984		T	34	GENIC	homozygous	137944703
7	29947326	29947334	TTTTGTCC		50	GENIC	homozygous	137944704
7	29948757	29948757		AGCGCTCTACCACTGAGCTAAATCCCCAGCC	37	GENIC	homozygous	137944705
7	29950501	29950501		AT	46	GENIC	homozygous	137944706
7	29951183	29951184	C	T	47	GENIC	homozygous	138049635
7	29951941	29951942	A	G	63	GENIC	homozygous	138049636
7	29952111	29952112	A	T	56	GENIC	homozygous	138049637
7	29944671	29944672	A		38	GENIC	possibly homozygous	403206135
7	29944671	29944672	A	C	38	GENIC	heterozygous	403206136
7	29952606	29952607	G	A	65	GENIC	homozygous	138049638