chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12653109	12653110	G	T	7	GENIC	homozygous	115570305
7	12653363	12653364	C	T	15	GENIC	homozygous	115570306
7	12653432	12653433	A	T	12	GENIC	homozygous	115570307
7	12653848	12653849	G	A	11	GENIC	possibly homozygous	115570308
7	12655016	12655017	T	G	21	GENIC	homozygous	115570309
7	12656228	12656229	T	C	23	GENIC	homozygous	115570310
7	12657656	12657657	G	A	23	GENIC	homozygous	115570312
7	12658970	12658971	G	A	30	GENIC	homozygous	115570313
7	12659703	12659704	T	C	22	GENIC	homozygous	115570315
7	12660224	12660225	T	C	17	GENIC	homozygous	115570316
7	12660243	12660244	A	G	15	GENIC	homozygous	115570317
7	12660535	12660536	C	T	16	GENIC	homozygous	118306912
7	12661132	12661133	C	T	16	GENIC	homozygous	115570318
7	12661270	12661271	A	G	16	GENIC	homozygous	115570319
7	12662169	12662170	A	T	8	GENIC	homozygous	115570320
7	12662402	12662403	C	T	16	GENIC	homozygous	115570321
7	12662445	12662446	T	C	13	GENIC	homozygous	115570322
7	12662466	12662467	G	A	7	GENIC	homozygous	115570323
7	12662510	12662511	C	G	6	GENIC	homozygous	115570324