chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12653109	12653110	G	T	42	GENIC	homozygous	115570305
7	12653363	12653364	C	T	41	GENIC	homozygous	115570306
7	12653432	12653433	A	T	43	GENIC	homozygous	115570307
7	12653820	12653820		G	28	GENIC	homozygous	128435832
7	12653848	12653849	G	A	27	GENIC	homozygous	115570308
7	12655016	12655017	T	G	44	GENIC	homozygous	115570309
7	12655497	12655498	C		44	GENIC	homozygous	128435833
7	12656228	12656229	T	C	62	GENIC	homozygous	115570310
7	12657265	12657266	C		25	GENIC	homozygous	128435834
7	12657267	12657270	TTC		25	GENIC	homozygous	128435835
7	12657284	12657284		T	26	GENIC	homozygous	128435836
7	12657656	12657657	G	A	11	GENIC	homozygous	115570312
7	12658762	12658762		GGGCCTTGCGCTTCCTAG	18	GENIC	homozygous	128435837
7	12658970	12658971	G	A	57	GENIC	homozygous	115570313
7	12659363	12659364	C		48	GENIC	possibly homozygous	128435838
7	12659703	12659704	T	C	38	GENIC	homozygous	115570315
7	12660224	12660225	T	C	35	GENIC	possibly homozygous	115570316
7	12660243	12660244	A	G	32	GENIC	homozygous	115570317
7	12660467	12660468	T	C	21	GENIC	heterozygous	131876573
7	12660469	12660470	G	A	21	GENIC	heterozygous	131876574
7	12660470	12660471	G	A	20	GENIC	heterozygous	131876575
7	12661132	12661133	C	T	69	GENIC	homozygous	115570318
7	12661270	12661271	A	G	85	GENIC	homozygous	115570319
7	12662169	12662170	A	T	84	GENIC	homozygous	115570320
7	12662445	12662446	T	C	66	GENIC	homozygous	115570322
7	12662466	12662467	G	A	71	GENIC	homozygous	115570323
7	12662510	12662511	C	G	72	GENIC	homozygous	115570324
7	12663775	12663775		G	56	GENIC	homozygous	128435839