chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	123584109	123584110	C	T	28	GENIC	homozygous	54236832
7	123584118	123584119	T	C	27	GENIC	homozygous	54236834
7	123584134	123584135	C	T	23	GENIC	homozygous	54236836
7	123584139	123584140	C	T	24	GENIC	homozygous	54236838
7	123584426	123584427	A	G	28	GENIC	heterozygous	54090385
7	123584457	123584458	A	G	33	GENIC	possibly homozygous	54090388
7	123584468	123584469	C	T	32	GENIC	possibly homozygous	54090390
7	123584484	123584485	G	A	29	GENIC	homozygous	54236840
7	123584770	123584771	C	T	29	GENIC	heterozygous	54090393
7	123585204	123585205	C	G	38	GENIC	homozygous	54236842
7	123585329	123585330	C	T	39	GENIC	homozygous	54090396
7	123586152	123586153	T	C	42	GENIC	homozygous	54090397
7	123586597	123586598	G	T	36	GENIC	homozygous	54236845
7	123586763	123586764	A	G	37	GENIC	homozygous	54090400
7	123587073	123587074	C	A	25	GENIC	homozygous	54090402
7	123587575	123587583	CATTCATT	--------	5	GENIC	homozygous	54090403
7	123587617	123587621	GTGT	----	10	GENIC	homozygous	54236847
7	123588203	123588204	T	-	4	GENIC	homozygous	54090407
7	123589080	123589081	A	G	32	GENIC	homozygous	54090412
7	123589463	123589464	C	T	30	GENIC	homozygous	54236849
7	123589702	123589703	T	C	3	GENIC	homozygous	54236850
7	123589989	123589990	C	T	17	GENIC	heterozygous	54236852
7	123592060	123592061	T	C	17	GENIC	heterozygous	54090413
7	123592064	123592065	T	C	17	GENIC	heterozygous	54090415