chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	65621999	65622003	TTTG		42	GENIC	homozygous	128825582
10	65623280	65623281	C	T	64	GENIC	homozygous	116619042
10	65623685	65623686	C	T	51	GENIC	homozygous	116619044
10	65626470	65626471	C	G	34	GENIC	homozygous	116619046
10	65627571	65627572	A	G	57	GENIC	homozygous	116619048
10	65628532	65628532		C	56	GENIC	homozygous	128825584
10	65629381	65629383	TG		35	GENIC	heterozygous	128825585
10	65629394	65629395	G		38	GENIC	homozygous	128825586
10	65629404	65629405	G		40	GENIC	homozygous	128825587
10	65630146	65630147	T	G	61	GENIC	homozygous	116619050
10	65630178	65630179	T	C	74	GENIC	homozygous	116619052
10	65630235	65630236	C	T	63	GENIC	homozygous	116619054
10	65631485	65631486	T	C	39	GENIC	homozygous	116619056
10	65631736	65631737	T		45	GENIC	homozygous	128825588
10	65631743	65631744	T	C	47	GENIC	homozygous	116619058
10	65632274	65632275	C	A	49	GENIC	homozygous	116619060
10	65632361	65632362	A	G	44	GENIC	homozygous	116619062
10	65632771	65632772	A	C	45	GENIC	homozygous	116619064
10	65629401	65629402	T	G	39	GENIC	possibly homozygous	128870752
10	65632842	65632843	G	A	40	GENIC	homozygous	116619066
10	65632952	65632953	G	A	48	GENIC	homozygous	116619068
10	65633093	65633094	G	A	46	GENIC	homozygous	116619070
10	65634047	65634048	C	T	55	GENIC	homozygous	116619072
10	65634453	65634454	T	C	59	GENIC	homozygous	116619074