chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	47067715	47067716	T	TC	20	GENIC	homozygous	45786968
20	47068020	47068021	A	G	39	GENIC	homozygous	45640496
20	47068122	47068123	G	T	34	GENIC	homozygous	45786969
20	47068380	47068381	T	C	31	GENIC	homozygous	45640497
20	47070656	47070657	C	T	38	GENIC	homozygous	45786972
20	47070879	47070880	C	T	38	GENIC	homozygous	45786973
20	47071999	47072000	T	C	34	GENIC	homozygous	45640505
20	47073141	47073145	ATAA	----	5	GENIC	homozygous	45852129
20	47069238	47069239	C	CAGG	31	GENIC	possibly homozygous	45852126
20	47069239	47069260	AGGAGGAGGGAGGACATCAGA	---------------------	31	GENIC	heterozygous	45852127
20	47069262	47069263	G	GAGGGAGGACATC	24	GENIC	heterozygous	45852128
20	47073495	47073496	C	CT	11	GENIC	homozygous	45582881
20	47073623	47073629	TGTGTG	------	13	GENIC	homozygous	45640508
20	47074335	47074336	C	T	17	GENIC	homozygous	45786974
20	47074503	47074521	CTCTCTCTCTCTCTCTCA	------------------	10	GENIC	heterozygous	45858028
20	47074505	47074521	CTCTCTCTCTCTCTCA	----------------	5	GENIC	heterozygous	45858029
20	47074535	47074536	A	AT	17	GENIC	homozygous	45786975
20	47074766	47074767	T	-	16	GENIC	homozygous	45640509
20	47074908	47074909	T	C	18	GENIC	homozygous	45640510