chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	122150594	122150595	G	C	59	GENIC	homozygous	54087457
7	122150826	122150827	C	CCA	19	GENIC	heterozygous	54087458
7	122152648	122152649	G	C	62	GENIC	heterozygous	54087459
7	122152761	122152762	G	A	107	GENIC	heterozygous	54087460
7	122152842	122152843	T	A	61	GENIC	heterozygous	54087461
7	122153042	122153043	T	C	40	GENIC	heterozygous	54087462
7	122153558	122153559	G	A	26	GENIC	homozygous	54087463
7	122155179	122155180	C	T	6	GENIC	heterozygous	54087464
7	122155180	122155181	A	AG	4	GENIC	homozygous	54087465
7	122155864	122155865	T	C	72	GENIC	homozygous	54087466
7	122156186	122156187	C	T	100	GENIC	heterozygous	54087467
7	122156212	122156213	A	G	93	GENIC	heterozygous	54087468
7	122156360	122156361	T	C	38	GENIC	heterozygous	54087469
7	122156381	122156382	T	A	31	GENIC	heterozygous	54087470
7	122156951	122156952	A	T	18	GENIC	homozygous	54087471
7	122157951	122157952	C	T	39	GENIC	homozygous	54087472
7	122158468	122158469	C	T	21	GENIC	possibly homozygous	54087473
7	122158658	122158659	T	C	40	GENIC	homozygous	54087474
7	122158661	122158662	A	G	40	GENIC	possibly homozygous	54087475
7	122163351	122163352	T	G	48	GENIC	heterozygous	54087476
7	122170066	122170067	T	-	25	GENIC	heterozygous	54087477
7	122173519	122173531	GTTTGTTTGTTT	------------	11	GENIC	homozygous	54087478