chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	71163968	71163969	A	G	51	GENIC	homozygous	114383681
13	71164587	71164588	C	T	50	GENIC	homozygous	114637506
13	71165364	71165364		C	11	GENIC	homozygous	131504008
13	71166576	71166577	T	C	39	GENIC	homozygous	114637508
13	71166577	71166578	G	A	40	GENIC	homozygous	114637510
13	71166671	71166672	G	A	35	GENIC	homozygous	114637512
13	71166305	71166305		AGGTT	46	GENIC	possibly homozygous	129069928
13	71166716	71166716		A	35	GENIC	homozygous	129069930
13	71166913	71166914	C	T	37	GENIC	homozygous	114383685
13	71166952	71166953	G	A	39	GENIC	homozygous	114637514
13	71167022	71167023	G	A	38	GENIC	homozygous	114637516
13	71167365	71167366	A	G	42	GENIC	homozygous	114383686
13	71167845	71167846	C	A	53	GENIC	homozygous	114637518
13	71169636	71169637	G	A	54	GENIC	homozygous	114637520
13	71169683	71169684	A	G	62	GENIC	homozygous	114383687
13	71169946	71169949	CTT		36	GENIC	homozygous	129069931
13	71169971	71169972	A	G	34	GENIC	homozygous	114383688
13	71170270	71170271	C	T	33	GENIC	homozygous	114383689
13	71171756	71171756		AGC	36	GENIC	homozygous	129069932
13	71176883	71176884	G	A	48	GENIC	homozygous	114383690
13	71178086	71178087	G	A	59	GENIC	homozygous	114637522
13	71178363	71178364	G	T	53	GENIC	homozygous	114637524