chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	52768081	52768082	C	CTTT	14	GENIC	homozygous	46409255
19	52769450	52769451	G	A	41	GENIC	homozygous	46159803
19	52769704	52769705	G	A	23	GENIC	homozygous	46159805
19	52769707	52769711	TATA	----	19	GENIC	homozygous	46159806
19	52771245	52771246	G	A	38	GENIC	homozygous	46159807
19	52771335	52771336	T	-	7	GENIC	heterozygous	46159809
19	52771459	52771460	T	TACACAC	7	GENIC	possibly homozygous	46159811
19	52771459	52771460	T	TACAC	7	GENIC	heterozygous	46409257
19	52771837	52771838	A	AT	10	GENIC	possibly homozygous	46159812
19	52771837	52771838	A	ATT	10	GENIC	heterozygous	46159814
19	52773531	52773532	A	T	24	GENIC	homozygous	46159815
19	52774754	52774755	A	G	35	GENIC	homozygous	46159817
19	52775516	52775517	T	TG	20	GENIC	heterozygous	46159818
19	52775752	52775753	C	T	15	GENIC	homozygous	46159820
19	52776150	52776151	C	CT	8	GENIC	heterozygous	46159821
19	52777981	52777982	A	G	54	GENIC	homozygous	46159823
19	52778279	52778280	T	C	33	GENIC	homozygous	46159824
19	52778370	52778371	G	GTGCTTGCTA	3	GENIC	homozygous	46409259
19	52778375	52778376	C	CAAG	6	GENIC	homozygous	46409261
19	52778377	52778378	G	GC	6	GENIC	homozygous	46409263
19	52778378	52778379	T	TCTACCACTGAGCTA	8	GENIC	homozygous	46409265
19	52778382	52778383	A	C	7	GENIC	homozygous	46409267
19	52778385	52778386	T	C	8	GENIC	homozygous	46409269
19	52778810	52778811	T	C	39	GENIC	homozygous	46159826
19	52778976	52778978	CT	--	26	GENIC	heterozygous	46463688
19	52779447	52779448	C	T	50	GENIC	homozygous	46159827
19	52782007	52782008	A	G	31	GENIC	homozygous	46159829
19	52782608	52782609	T	C	29	GENIC	homozygous	46159830
19	52783154	52783155	G	GTGTGTGTGTGTA	19	GENIC	possibly homozygous	46381277
19	52776150	52776151	C	CTT	8	GENIC	heterozygous	46446229
19	52778328	52778329	C	CT	9	GENIC	heterozygous	46553301