chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	122267472	122267473	C	T	28	GENIC	homozygous	115860348
7	122281013	122281014	A	T	19	GENIC	homozygous	118259200
7	122281014	122281015	G	A	19	GENIC	homozygous	118259202
7	122302396	122302397	A	G	16	GENIC	homozygous	115860352
7	122312981	122312982	C	A	26	GENIC	homozygous	115860354
7	122313196	122313197	T	A	23	GENIC	homozygous	115860356
7	122321411	122321412	A	G	8	GENIC	possibly homozygous	116082058
7	122338427	122338428	G	A	23	GENIC	homozygous	118322276
7	122299271	122299272	A	C	16	GENIC	heterozygous	118322270
7	122306116	122306117	C	A	20	GENIC	homozygous	118322272
7	122320498	122320499	C	A	21	GENIC	heterozygous	118322274
7	122346584	122346585	A	G	20	GENIC	homozygous	115860358
7	122347648	122347649	C	A	28	GENIC	homozygous	115860360
7	122347726	122347727	A	G	23	GENIC	homozygous	116226015
7	122347812	122347813	C	A	34	GENIC	homozygous	115860362
7	122358368	122358369	A	G	33	GENIC	homozygous	116226043
7	122375424	122375425	C	T	30	GENIC	homozygous	118259206
7	122375425	122375426	T	A	30	GENIC	homozygous	118259208
7	122378672	122378673	A	G	43	GENIC	homozygous	116082063
7	122378673	122378674	A	T	43	GENIC	homozygous	116082064
7	122378674	122378675	A	C	42	GENIC	homozygous	116082065